Name

Heiser et al., PNAS, 2011 Cell Line Gene Expression Profiles Dataset

From Heiser et al., PNAS, 2011

mRNA expression profiles for breast cancer cell lines measured by microarray

Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles Dataset

From Klijn et al., Nat. Biotechnol., 2015

gene-level copy number variation profiles for cancer cell lines

Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles Dataset

From Klijn et al., Nat. Biotechnol., 2015

mRNA expression profiles for cancer cell lines

Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles Dataset

From Klijn et al., Nat. Biotechnol., 2015

gene mutations in cancer cell lines

RNU7-24P Gene

RNA, U7 small nuclear 24 pseudogene

RNU1-28P Gene

RNA, U1 small nuclear 28, pseudogene

MIR4435-2HG Gene

MIR4435-2 host gene

RNU1-20P Gene

RNA, U1 small nuclear 20, pseudogene

LL0XNC01-250H12.3 Gene

uncharacterized LOC100506901

GS1-259H13.2 Gene

transmembrane protein 225-like

WI2-2373I1.2 Gene

forkhead box L1-like

RNU7-27P Gene

RNA, U7 small nuclear 27 pseudogene

RNU6-21P Gene

RNA, U6 small nuclear 21, pseudogene

CTD-2201I18.1 Gene

uncharacterized LOC101929215

RNU1-27P Gene

RNA, U1 small nuclear 27, pseudogene

RNU7-28P Gene

RNA, U7 small nuclear 28 pseudogene

CTD-2337A12.1 Gene

CTD-2194D22.4 Gene

uncharacterized LOC101929081

RNU7-22P Gene

RNA, U7 small nuclear 22 pseudogene

RNU6-26P Gene

RNA, U6 small nuclear 26, pseudogene

RNU1-22P Gene

RNA, U1 small nuclear 22, pseudogene

TRAV38-2DV8 Gene

T cell receptor alpha variable 38-2/delta variable 8

RNU7-25P Gene

RNA, U7 small nuclear 25 pseudogene

RNU6-23P Gene

RNA, U6 small nuclear 23, pseudogene

RNU7-20P Gene

RNA, U7 small nuclear 20 pseudogene

RNU1-21P Gene

RNA, U1 small nuclear 21, pseudogene

GS1-278J22.2 Gene

uncharacterized LOC105375283

LL21NC02-21A1.1 Gene

uncharacterized LOC101928745

CTD-2154B17.1 Gene

uncharacterized CTD-2154B17.1

RNU1-24P Gene

RNA, U1 small nuclear 24, pseudogene

CTD-2151A2.1 Gene

uncharacterized LOC102724855

RNU7-23P Gene

RNA, U7 small nuclear 23 pseudogene

DUPXP11.23P11.22 Gene

Chromosome Xp11.23-p11.22 duplication syndrome

CTD-2201E9.1 Gene

uncharacterized LOC101929338

GS1-204I12.4 Gene

uncharacterized LOC105371653

CH507-210P18.4 Gene

uncharacterized LOC105372737

GS1-24F4.2 Gene

uncharacterized LOC100652791

CTD-2270F17.1 Gene

uncharacterized LOC101928033

RNU7-26P Gene

RNA, U7 small nuclear 26 pseudogene

CTD-2350J17.1 Gene

uncharacterized LOC101929472

IGKV3OR2-268 Gene

immunoglobulin kappa variable 3/OR2-268 (non-functional)

CTD-2297D10.2 Gene

uncharacterized LOC101929176

GS1-251I9.3 Gene

uncharacterized LOC105375636

MIR124-2HG Gene

MIR124-2 host gene

CTD-2118P12.1 Gene

RNU7-29P Gene

RNA, U7 small nuclear 29 pseudogene

RNU6-28P Gene

RNA, U6 small nuclear 28, pseudogene

RNU7-21P Gene

RNA, U7 small nuclear 21 pseudogene

GS1-279B7.1 Gene

microtubule-associated protein 1 light chain 3 beta pseudogene

SMAR Gene

Spinal muscular atrophy, chronic distal, autosomal recessive

SMAL Gene

spinal muscular atrophy, congenital nonprogressive, of lower limbs

SMAJ Gene

Spinal muscular atrophy, Jokela type

SCA18 Gene

spinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy)

MDRV Gene

muscular dystrophy, with rimmed vacuoles

MLIP Gene

muscular LMNA-interacting protein

LGMD1H Gene

limb girdle muscular dystrophy 1H (autosomal dominant)

LGMD1G Gene

limb girdle muscular dystrophy 1G (autosomal dominant)

MDC1B Gene

Muscular dystrophy, congenital, 1B

FSHMD1A Gene

facioscapulohumeral muscular dystrophy 1A

Facioscapulohumeral muscular dystrophy (FSHD) is a common hereditary disease of muscle. Patients with FSHD have a chromosomal rearrangement within the subtelomeric region of chromosome 4 (4q35). This region is composed mainly of a polymorphic repeat structure consisting of 3.3 kb repeat units, designated D4Z4. The number of repeat units varies from 10 to more than 100 in the population, however, in FSHD patients only 1-10 repeat units is observed because of a deletion of an integral number of these units. FSHD is caused by an epigenetic mechanism involving the contraction of a subtelomeric macrosatellite repeat, which results in marked hypomethylation of the contracted D4Z4 allele. It is likely not the structure, but the deregulation of transcription of one or more genes as a result of repeat-contraction-mediated chromatin alterations, that causes FSHD. [provided by RefSeq, Sep 2011]

FSHMD1B Gene

facioscapulohumeral muscular dystrophy 1B

MDCMP Gene

muscular dystrophy, congenital, merosin-positive

OPA6 Gene

optic atrophy 6 (autosomal recessive)

OPA4 Gene

optic atrophy 4 (autosomal dominant)

OPA5 Gene

optic atrophy 5 (autosomal dominant)

OPA2 Gene

optic atrophy 2 (obscure)

OPA1 Gene

optic atrophy 1 (autosomal dominant)

This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

OPA3 Gene

optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)

The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]

PBCRA1 Gene

progressive bifocal chorioretinal atrophy 1

SPOAN Gene

spastic paraplegia, optic atrophy, and neuropathy

CLAM Gene

cerebellar atrophy with progressive microcephaly

LOAS Gene

Leber optic atrophy, susceptibility to

spinal muscular atrophy-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular atrophy, spinal; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Spinal muscular atrophy, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, X-linked 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, autosomal recessive 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, Jerash type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy with respiratory distress 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.

Muscular Atrophy, Spinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

adult spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intermediate spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

survival motor neuron spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular atrophy, spinal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Muscular Atrophy, Spinal Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy with progressive myoclonic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, x-linked 2, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, chronic distal, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, jokela type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal spinal muscular atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, late-onset, finkel type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.

{spinal muscular atrophy, type iii, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, x-linked 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal and bulbar muscular atrophy of kennedy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, congenital nonprogressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal canal and spinal cord meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal canal and spinal cord meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord compression; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal cord compression; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Spinal Cord Injury_CNS - Spinal Cord (MMHCC)_GSE16710 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Spinal Cord Injury_CNS - Spinal Cord (MMHCC)_GSE16710 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

atrophy/degeneration involving the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy of the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Spinal Muscular Atrophies of Childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.

spinal muscular atrophies of childhood Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Spinal Muscular Atrophies of Childhood Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Muscular Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset.

muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

progressive muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular atrophy; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular atrophy Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

progressive distal muscular atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nonprogressive muscular atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Muscular Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

decreased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease becker muscular dystrophy; duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophies; muscular dystrophies, limb-girdle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies; muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal trigeminal nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal trigeminal nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

spinal trigeminal nucleus, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal trigeminal nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

r8 part of spinal trigeminal nucleus, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r8 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r9 part of spinal trigeminal nucleus, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r9 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r6 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r6 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, rostral dorsomedial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, rostral dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r10 part of spinal trigeminal nucleus, caudal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r10 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r6 part of spinal trigeminal nucleus, pars oralis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r6 part of spinal trigeminal nucleus, pars oralis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r3 part of spinal trigeminal sensory column, oral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r3 part of spinal trigeminal sensory column, oral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r10 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r10 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r7 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r7 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, dorsal zone Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, dorsal zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r11 part of spinal trigeminal nucleus, caudal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r11 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r5 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r5 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r7 part of spinal trigeminal nucleus, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r7 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r8 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r8 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, caudal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, ventrolateral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, ventrolateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r9 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r9 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, ventral zone Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, ventral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

spinal trigeminal nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal trigeminal nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

spinal (inferior) vestibular nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal (inferior) vestibular nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Neurofibromatosis, familial spinal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Spinal Curvatures Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Curvatures from the curated CTD Gene-Disease Associations dataset.

Spinal Dysraphism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Dysraphism from the curated CTD Gene-Disease Associations dataset.

Spinal Cord Injuries Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Cord Injuries from the curated CTD Gene-Disease Associations dataset.

Spinal Cord Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Cord Diseases from the curated CTD Gene-Disease Associations dataset.

Spinal Cord Ischemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Cord Ischemia from the curated CTD Gene-Disease Associations dataset.

Neurofibromatosis, Familial Spinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.

Spinal Cord Compression Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Cord Compression from the curated CTD Gene-Disease Associations dataset.

Hematoma, Epidural, Spinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hematoma, Epidural, Spinal from the curated CTD Gene-Disease Associations dataset.

spinal cord glioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal stenosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior spinal artery syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior spinal artery syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord astrocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

tethered spinal cord syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease tethered spinal cord syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord ependymoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal chordoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal chordoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal canal intradural extramedullary neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal canal intradural extramedullary neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord oligodendroglioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal cord primitive neuroectodermal neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinal cord primitive neuroectodermal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

H3K4me3_astrocyte of the spinal cord_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_astrocyte of the spinal cord_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_astrocyte of the spinal cord_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_astrocyte of the spinal cord_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

CTCF_astrocyte of the spinal cord_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_astrocyte of the spinal cord_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_astrocyte of the spinal cord_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_astrocyte of the spinal cord_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tuberculosis, spinal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tuberculosis, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute traumatic spinal cord injury Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute traumatic spinal cord injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; intervertebral disk displacement; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; intervertebral disk displacement; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal cord injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal cord diseases; spondylosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal cord diseases; spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal cord infarction and recurrent venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal cord infarction and recurrent venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acoustic neurofibromatosis; meningioma; neurofibromatosis 2; spinal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acoustic neurofibromatosis; meningioma; neurofibromatosis 2; spinal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; low back pain; scoliosis; spinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; low back pain; scoliosis; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal ossification Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal ossification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

paralysis; sensation disorders; spinal cord injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease paralysis; sensation disorders; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism disorders; obesity; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose metabolism disorders; obesity; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal disc degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; osteoporosis; spinal injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain hypoxia; burns; hypoxia, brain; spinal cord injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain hypoxia; burns; hypoxia, brain; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cushing syndrome; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cushing syndrome; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meningomyelocele; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meningomyelocele; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; hip fractures; osteoporosis; spinal injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; hip fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; spinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term spinal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

smoothened signaling pathway involved in spinal cord motor neuron cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations dataset.

spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

spinal cord ventral commissure morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord ventral commissure morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron specification Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord development Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord development biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in ventral spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification biological process from the curated GO Biological Process Annotations dataset.

negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

commissural neuron differentiation in spinal cord Gene Set

From GO Biological Process Annotations

genes participating in the commissural neuron differentiation in spinal cord biological process from the curated GO Biological Process Annotations dataset.

spinal cord motor neuron cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in ventral spinal cord interneuron specification Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations dataset.

spinal cord association neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord association neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter involved in ventral spinal cord interneuron specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron fate commitment biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter involved in spinal cord association neuron specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord association neuron specification biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron differentiation biological process from the curated GO Biological Process Annotations dataset.

musculoskeletal movement, spinal reflex action Gene Set

From GO Biological Process Annotations

genes participating in the musculoskeletal movement, spinal reflex action biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron fate determination Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron fate determination biological process from the curated GO Biological Process Annotations dataset.

cell differentiation in spinal cord Gene Set

From GO Biological Process Annotations

genes participating in the cell differentiation in spinal cord biological process from the curated GO Biological Process Annotations dataset.

bmp signaling pathway involved in spinal cord dorsal/ventral patterning Gene Set

From GO Biological Process Annotations

genes participating in the bmp signaling pathway involved in spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations dataset.

dorsal spinal cord development Gene Set

From GO Biological Process Annotations

genes participating in the dorsal spinal cord development biological process from the curated GO Biological Process Annotations dataset.

spinal cord anterior/posterior patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations dataset.

spinal cord dorsal/ventral patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations dataset.

spinal cord motor neuron migration Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations dataset.

corticospinal neuron axon guidance through spinal cord Gene Set

From GO Biological Process Annotations

genes participating in the corticospinal neuron axon guidance through spinal cord biological process from the curated GO Biological Process Annotations dataset.

spinal cord development Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord development biological process from the curated GO Biological Process Annotations dataset.

spinal cord motor neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

spinal cord oligodendrocyte cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord oligodendrocyte cell fate specification biological process from the curated GO Biological Process Annotations dataset.

abnormality of the spinal cord Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

spinal rigidity Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the spinal rigidity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

widening of cervical spinal canal Gene Set

From HPO Gene-Disease Associations

genes associated with the widening of cervical spinal canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal dysraphism Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal dysraphism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic spinal processes Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic spinal processes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetry of spinal facet joints Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetry of spinal facet joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the dorsal column of the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the dorsal column of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal rigidity Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal rigidity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal canal stenosis Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal canal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord compression Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal cord compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the spinal meninges Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the spinal meninges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal stenosis with reduced interpedicular distance Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal stenosis with reduced interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pallor of dorsal columns of the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the pallor of dorsal columns of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal deformities Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal deformities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal hemangioblastoma Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal hemangioblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal instability Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal instability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord posterior columns myelin loss Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal neurofibromas Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal neurofibromas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symmetric spinal nerve root neurofibromas Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetric spinal nerve root neurofibromas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal cord lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord tumor Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal cord tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cervical spinal canal stenosis Gene Set

From HPO Gene-Disease Associations

genes associated with the cervical spinal canal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Spinal Dysraphism Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Dysraphism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Cord Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Cord Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Osteophytosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Osteophytosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Stenosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Injuries Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Injuries phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Tuberculosis, Spinal Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Tuberculosis, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal spinal cord dorsal column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord dorsal column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord white matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord dorsal horn morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord dorsal horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord grey matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord grey matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal nerve morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord central canal morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord ventral horn morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord ventral horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spinal cord size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord interneuron morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord interneuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased spinal cord size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord ventral commissure morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord ventral commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord motor column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord lateral column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord lateral column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord lateral motor column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord lateral motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord ependymal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord ependymal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spinal cord degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord commissure morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ventral spinal root morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ventral spinal root morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spinal cord ventral horn cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spinal cord ventral horn cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spinal hemorrhage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased spinal cord apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased spinal cord apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal dorsal spinal root morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal dorsal spinal root morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal reflex Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

neurofibromatosis, familial spinal Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurofibromatosis, familial spinal phenotype from the curated OMIM Gene-Disease Associations dataset.

TWIK-related spinal cord K+ channel (TRESK) Gene Set

From Reactome Pathways

proteins participating in the TWIK-related spinal cord K+ channel (TRESK) pathway from the Reactome Pathways dataset.

spinal column Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal column from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

spinal cord Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal cord from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

spinal ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

spinal cord Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal cord in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

spinal ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

spinal column Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue spinal column in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior spinal root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

spinal nerve Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue spinal nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

spinal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue spinal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

spinal trigeminal tract Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue spinal trigeminal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

spinal muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue spinal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

posterior spinal root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue posterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

spinal cord Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue spinal cord in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

spinal root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Spinal Cord Injury(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Spinal Cord Injury(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Spinal Cord Injury(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Spinal Cord Injury(Mus musculus) pathway from the Wikipathways Pathways dataset.

Bosch-boonstra-schaaf optic atrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dominant hereditary optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked myopathy with postural muscle atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic Atrophy Type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital microvillous atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sveinsson Chorioretinal Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy, Hereditary, Leber Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 1 and deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.

Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrophy from the curated CTD Gene-Disease Associations dataset.

Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset.

Costeff optic atrophy syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset.

Optic atrophy polyneuropathy deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.

Chorioretinal atrophy, progressive bifocal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Gyrate Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gyrate Atrophy from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset.

Pigmented Paravenous Chorioretinal Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.

OPTIC ATROPHY 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

dentatorubral-pallidoluysian atrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

multiple system atrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

atrophy of prostate Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

primary optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

skin atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atrophy of testis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple system atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hereditary choroidal atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

dentatorubral-pallidoluysian atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

partial optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

olivopontocerebellar atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

gyrate atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

choroidal neovascularization; geographic atrophy; macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; dementia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; gastritis; helicobacter infections; metaplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; geographic atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroidal neovascularization; geographic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

posterior cortical atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

geographic atrophy; macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; helicobacter infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; prenatal exposure delayed effects; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; prenatal exposure delayed effects; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic disc atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gyrate atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gyrate atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

geographic atrophy; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; peptic ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; brain diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; choroidal neovascularization; macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; gastritis; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; gastritis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; aphasia; atrophy; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; aphasia; atrophy; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; multiple sclerosis, relapsing-remitting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastric atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastric atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, hereditary, leber; vision disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; amnesia; atrophy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; amnesia; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stomach cancer; stomach atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stomach cancer; stomach atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; atrophy; brain diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; epilepsy; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy and moderate deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; gastritis; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; brain atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; huntington disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hippocampal atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hippocampal atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonic disorders; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term atrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

skeletal muscle atrophy Gene Set

From GO Biological Process Annotations

genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations dataset.

positive regulation of muscle atrophy Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations dataset.

regulation of muscle atrophy Gene Set

From GO Biological Process Annotations

genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations dataset.

striated muscle atrophy Gene Set

From GO Biological Process Annotations

genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations dataset.

muscle atrophy Gene Set

From GO Biological Process Annotations

genes participating in the muscle atrophy biological process from the curated GO Biological Process Annotations dataset.

MRI atrophy measures Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the MRI atrophy measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hippocampal atrophy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

motor neuron atrophy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the motor neuron atrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

atrophy/degeneration affecting the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

type 2 muscle fiber atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the type 2 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

levator palpebrae superioris atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the levator palpebrae superioris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral white matter atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy/degeneration affecting the central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar cortical atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy/degeneration involving the corticospinal tracts Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized limb muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

global brain atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the global brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral retinal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

caudate atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the caudate atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corpus callosum atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the corpus callosum atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tubular atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thenar muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the thenar muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pontocerebellar atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the pontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse cerebellar atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

brain atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skeletal muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tongue atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the tongue atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

olivopontocerebellar atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the olivopontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dermal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripapillary chorioretinal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontal cortical atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subcortical cerebral atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscle fiber atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse skin atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hand muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

motor neuron atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pelvic girdle muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the pelvic girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

leber optic atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral axonal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

retinal pigment epithelial atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fundus atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the fundus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scapular muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the scapular muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy/degeneration affecting the cerebrum Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

first dorsal interossei muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the first dorsal interossei muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy/degeneration affecting the brainstem Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy/degeneration involving the caudate nucleus Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic atrophy from cranial nerve compression Gene Set

From HPO Gene-Disease Associations

genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar vermis atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

villous atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

iris atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy of alveolar ridges Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy of alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

interosseus muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the interosseus muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

type 1 muscle fiber atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral cortical atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

superior rectus atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

noninflammatory macular atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized cerebral atrophy/hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse cerebral atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

limb-girdle muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

testicular atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the testicular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shoulder girdle muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the shoulder girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pigmented paravenous chorioretinal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the pigmented paravenous chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal cortical atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peroneal muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the peroneal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chorioretinal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontotemporal cerebral atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the frontotemporal cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy of the dentate nucleus Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

quadriceps muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the quadriceps muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinocerebellar atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the spinocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

retinal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

temporal cortical atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the temporal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple System Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophy, Hereditary, Leber Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophy, Autosomal Dominant Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Geographic Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Geographic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic atrophy 3-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

dentatorubropallidoluysian atrophy Gene Set

From KEGG Pathways

proteins participating in the dentatorubropallidoluysian atrophy pathway from the KEGG Pathways dataset.

ovary atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle fiber atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney cortex atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

testicular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the testicular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney collecting duct atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thymus atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thymus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brain atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the brain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic nerve atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal pigment epithelium atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sebaceous gland atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

midbrain atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

renal tubule atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

seminal vesicle atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

renal glomerulus atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

meibomian gland atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the meibomian gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

uterus atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pancreatic acinar cell atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

endometrium atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

epidermal atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

exocrine pancreas atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spleen atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

iris atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the iris atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vagina atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vagina atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vulva atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vulva atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pancreas atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

oviduct atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

external male genitalia atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney medulla atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney papillary atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic atrophy 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy-4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple system atrophy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, x-linked, with postural muscle atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

sveinsson choreoretinal atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the sveinsson choreoretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

dentatorubro-pallidoluysian atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the dentatorubro-pallidoluysian atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy-7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia, optic atrophy, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

bosch-boonstra-schaaf optic atrophy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 2, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

gyrate atrophy of choroid and retina with or without ornithinemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 3 with cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

pigmented paravenous chorioretinal atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

?neurodegeneration with optic atrophy, childhood onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy plus syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

{leber optic atrophy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

Duchenne muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Merosin deficient congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Walker-Warburg congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2S Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Becker muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facioscapulohumeral muscular dystrophy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-dreifuss muscular dystrophy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ullrich congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular hypertrophy-cerebral syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Miyoshi Muscular Dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Miyoshi Muscular Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miyoshi Muscular Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.

Facioscapulohumeral muscular dystrophy 1a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophies, Limb-Girdle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophies, Limb-Girdle from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Animal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy congenital, merosin negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.

Scleroatonic muscular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scleroatonic muscular dystrophy from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Emery-Dreifuss Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophies from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Facioscapulohumeral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Oculopharyngeal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.

Muscular Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Diseases from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Merosin-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.

Facioscapulohumeral Muscular Dystrophy 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy, limb-girdle, type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Duchenne Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Lmna-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.

Limb-Girdle Muscular Dystrophy, Type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.

Muscular Diseases Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Muscular Diseases in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

limb-girdle muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

atrophic muscular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease atrophic muscular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ullrich congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

muscular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease muscular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

muscular disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease muscular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

atrophic muscular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease atrophic muscular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

distal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

limb-girdle muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ullrich congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

becker muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease emery-dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

duchenne muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophy-dystroglycanopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease muscular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophies, limb-girdle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; glucose intolerance; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy, oculopharyngeal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophy, oculopharyngeal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism disorders; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipid metabolism disorders; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ullrich congenital muscular dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ullrich congenital muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular disorders, atrophic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular disorders, atrophic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; hypercholesterolemia; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; hypercholesterolemia; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term muscular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

muscular septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the muscular septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

muscular disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease muscular disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

muscular hypotonia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscular hypotonia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

limb-girdle muscular dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital muscular torticollis Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital muscular torticollis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

extrapyramidal muscular rigidity Gene Set

From HPO Gene-Disease Associations

genes associated with the extrapyramidal muscular rigidity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular edema Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile muscular hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular hypotonia of the trunk Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular hypotonia of the trunk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe muscular hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the severe muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital muscular dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized muscular appearance from birth Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Muscular Dystrophies, Limb-Girdle Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophies, Limb-Girdle phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Disorders, Atrophic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Disorders, Atrophic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Dystrophy, Emery-Dreifuss Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Dystrophies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Dystrophy, Facioscapulohumeral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Facioscapulohumeral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Dystrophy, Duchenne Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Duchenne phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular LMNA-interacting protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Muscular LMNA-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small muscular protein Chisel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small muscular protein Chisel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal interventricular septum muscular part morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal interventricular septum muscular part morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fascioscapulohumeral muscular dystrophy 2, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, megaconial type Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?muscular dystrophy, limb-girdle, type 2r Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, rigid spine, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, merosin-positive Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2q Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2s Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2g Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2l Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2j Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.

ullrich congenital muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

tibial muscular dystrophy, tardive Gene Set

From OMIM Gene-Disease Associations

genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.

oculopharyngeal muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

duchenne muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 3, ar Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

limb-girdle muscular dystrophy, type 1g Gene Set

From OMIM Gene-Disease Associations

genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy with rimmed vacuoles Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 6, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy with epidermolysis bullosa simplex Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy with epidermolysis bullosa simplex phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

becker muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 7, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital merosin-deficient Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

vertebrate muscular system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue vertebrate muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

muscular system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

vertebrate muscular system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue vertebrate muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

muscular coat Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue muscular coat in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

invertebrate muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue invertebrate muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

vertebrate muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue vertebrate muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Emery-Dreifuss muscular dystrophy Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

TG(20:2n6/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/o-18:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/o-18:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:3n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:3n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/24:1(15Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/24:1(15Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:1(11Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:1(11Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/18:4(6Z,9Z,12Z,15Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/18:4(6Z,9Z,12Z,15Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:0/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:0/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(18:2n6/0:0/22:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(18:2n6/0:0/22:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:1(11Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:1(11Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/20:5(5Z,8Z,11Z,14Z,17Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/20:5(5Z,8Z,11Z,14Z,17Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:4(8Z,11Z,14Z,17Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:4(8Z,11Z,14Z,17Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:1(9Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:1(9Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/18:3(9Z,12Z,15Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/18:3(9Z,12Z,15Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(16:1(9Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(16:1(9Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/14:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/14:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:0/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:0/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/20:4(5Z,8Z,11Z,14Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/20:4(5Z,8Z,11Z,14Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/14:1(9Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/14:1(9Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/18:4(6Z,9Z,12Z,15Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/18:4(6Z,9Z,12Z,15Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/22:4(7Z,10Z,13Z,16Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/22:4(7Z,10Z,13Z,16Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/22:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/22:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/22:5(7Z,10Z,13Z,16Z,19Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/22:5(7Z,10Z,13Z,16Z,19Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/18:3(6Z,9Z,12Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/18:3(6Z,9Z,12Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(24:1(15Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(24:1(15Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/22:5(4Z,7Z,10Z,13Z,16Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/22:5(4Z,7Z,10Z,13Z,16Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(22:1(13Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(22:1(13Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/22:4(7Z,10Z,13Z,16Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/22:4(7Z,10Z,13Z,16Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(22:0/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(22:0/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/22:2(13Z,16Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/22:2(13Z,16Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/24:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/24:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:5(5Z,8Z,11Z,14Z,17Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:5(5Z,8Z,11Z,14Z,17Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:3(5Z,8Z,11Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:3(5Z,8Z,11Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(15:0/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(15:0/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(14:1(9Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(14:1(9Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(20:2n6/0:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(20:2n6/0:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/16:1(9Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/16:1(9Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(14:0/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(14:0/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(18:2n6/0:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(18:2n6/0:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:1(11Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:1(11Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/22:2(13Z,16Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/22:2(13Z,16Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(18:2n6/0:0/18:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(18:2n6/0:0/18:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/16:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/16:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(16:0/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(16:0/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(20:2n6/0:0/22:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(20:2n6/0:0/22:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/18:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/18:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/o-18:0) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/o-18:0) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/15:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/15:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:3(6Z,9Z,12Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:3(6Z,9Z,12Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/18:1(11Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/18:1(11Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(24:0/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(24:0/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/22:1(13Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/22:1(13Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/18:2(9Z,12Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/18:2(9Z,12Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/18:1(9Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/18:1(9Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/22:5(7Z,10Z,13Z,16Z,19Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/22:5(7Z,10Z,13Z,16Z,19Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/20:4(8Z,11Z,14Z,17Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/20:4(8Z,11Z,14Z,17Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:2(9Z,12Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:2(9Z,12Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(22:2n6/0:0/22:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(22:2n6/0:0/22:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:0/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:0/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3(5Z,8Z,11Z)/20:2n6/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3(5Z,8Z,11Z)/20:2n6/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:4(5Z,8Z,11Z,14Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:4(5Z,8Z,11Z,14Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:2n6/18:3(9Z,12Z,15Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:2n6/18:3(9Z,12Z,15Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/22:5(4Z,7Z,10Z,13Z,16Z)/20:2n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/22:5(4Z,7Z,10Z,13Z,16Z)/20:2n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

22RV1 Gene Set

From Achilles Cell Line Gene Essentiality Profiles

gene knockdowns changing fitness of 22RV1 relative to other cell lines from the Achilles Cell Line Gene Essentiality Profiles dataset.

posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_21 pcw_F_12365 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 Gene Set

From