Name

CTD Gene-Chemical Interactions Dataset

From Comparative Toxicogenomics Database

chemical-gene interactions curated from literature

CTD Gene-Disease Associations Dataset

From Comparative Toxicogenomics Database

disease-gene interactions curated from literature

TONSL-AS1 Gene

TONSL antisense RNA 1

TOM1L2 Gene

target of myb1-like 2 (chicken)

TOMM40 Gene

translocase of outer mitochondrial membrane 40 homolog (yeast)

TOMM40 is the channel-forming subunit of the translocase of the mitochondrial outer membrane (TOM) complex that is essential for protein import into mitochondria (Humphries et al., 2005 [PubMed 15644312]).[supplied by OMIM, May 2008]

TOB2 Gene

transducer of ERBB2, 2

TOB2 belongs to the TOB (see TOB1; MIM 605523)/BTG1 (MIM 109580) family of antiproliferative proteins, which are involved in the regulation of cell cycle progression.[supplied by OMIM, Apr 2004]

TOPAZ1 Gene

testis and ovary specific PAZ domain containing 1

TOMM40L Gene

translocase of outer mitochondrial membrane 40 homolog (yeast)-like

TOMM6 Gene

translocase of outer mitochondrial membrane 6 homolog (yeast)

TOMM7 Gene

translocase of outer mitochondrial membrane 7 homolog (yeast)

This gene encodes a subunit of the translocase of the outer mitochondrial membrane. The encoded protein regulates the assembly and stability of the translocase complex. [provided by RefSeq, Oct 2012]

TOMM5 Gene

translocase of outer mitochondrial membrane 5 homolog (yeast)

TOP3BP1 Gene

topoisomerase (DNA) III beta pseudogene 1

This gene was predicted by automated computational analysis. It encodes a protein with similarity to human topoisomerase (DNA) III beta, which is thought to relax supercoiled DNA upon replication, transcription, and cell division. This gene lies in the immunoglobulin lambda gene cluster on chromosome 22q11.21. [provided by RefSeq, Jul 2008]

TOPORS Gene

topoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase

This gene encodes a nuclear protein which is serine and arginine rich, and contains a RING-type zinc finger domain. It is highly expressed in the testis, and functions as an ubiquitin-protein E3 ligase. Mutations in this gene are associated with retinitis pigmentosa type 31. Alternatively spliced transcript variants, encoding different isoforms, have been observed for this locus. [provided by RefSeq, Sep 2010]

TOB1-AS1 Gene

TOB1 antisense RNA 1

TOPORS-AS1 Gene

TOPORS antisense RNA 1

TOR2A Gene

torsin family 2, member A

This gene encodes a member of the AAA family of adenosine triphosphatases with similarity to Clp proteases and heat shock proteins. Alternative splicing at this locus results in the translation of multiple isoforms of the encoded protein, some of which contain salusin peptides in the C-terminal region. These peptides may play roles in hypotension, myocardial growth and the induction of mitogenesis, and may also be involved in the pathogenesis of atherosclerosis. The antimicrobial peptide salusin-beta has antibacterial activity. [provided by RefSeq, Nov 2014]

TOPORSLP Gene

topoisomerase I binding, arginine/serine-rich like, pseudogene

TOMM20 Gene

translocase of outer mitochondrial membrane 20 homolog (yeast)

TOMM22 Gene

translocase of outer mitochondrial membrane 22 homolog (yeast)

The protein encoded by this gene is an integral membrane protein of the mitochondrial outer membrane. The encoded protein interacts with TOMM20 and TOMM40, and forms a complex with several other proteins to import cytosolic preproteins into the mitochondrion. [provided by RefSeq, Jul 2008]

TOP2B Gene

topoisomerase (DNA) II beta 180kDa

This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This nuclear enzyme is involved in processes such as chromosome condensation, chromatid separation, and the relief of torsional stress that occurs during DNA transcription and replication. It catalyzes the transient breaking and rejoining of two strands of duplex DNA which allows the strands to pass through one another, thus altering the topology of DNA. Two forms of this enzyme exist as likely products of a gene duplication event. The gene encoding this form, beta, is localized to chromosome 3 and the alpha form is localized to chromosome 17. The gene encoding this enzyme functions as the target for several anticancer agents and a variety of mutations in this gene have been associated with the development of drug resistance. Reduced activity of this enzyme may also play a role in ataxia-telangiectasia. Alternative splicing of this gene results in two transcript variants; however, the second variant has not yet been fully described. [provided by RefSeq, Jul 2008]

TOP2A Gene

topoisomerase (DNA) II alpha 170kDa

This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This nuclear enzyme is involved in processes such as chromosome condensation, chromatid separation, and the relief of torsional stress that occurs during DNA transcription and replication. It catalyzes the transient breaking and rejoining of two strands of duplex DNA which allows the strands to pass through one another, thus altering the topology of DNA. Two forms of this enzyme exist as likely products of a gene duplication event. The gene encoding this form, alpha, is localized to chromosome 17 and the beta gene is localized to chromosome 3. The gene encoding this enzyme functions as the target for several anticancer agents and a variety of mutations in this gene have been associated with the development of drug resistance. Reduced activity of this enzyme may also play a role in ataxia-telangiectasia. [provided by RefSeq, Jul 2010]

TOMM22P2 Gene

TOMM22 pseudogene 2

TOMM20P2 Gene

TOMM20 pseudogene 2

TOMM20P4 Gene

TOMM20 pseudogene 4

TOR1A Gene

torsin family 1, member A (torsin A)

The protein encoded by this gene is a member of the AAA family of adenosine triphosphatases (ATPases), is related to the Clp protease/heat shock family and is expressed prominently in the substantia nigra pars compacta. Mutations in this gene result in the autosomal dominant disorder, torsion dystonia 1. [provided by RefSeq, Jul 2008]

TOR1B Gene

torsin family 1, member B (torsin B)

TOMM70A Gene

translocase of outer mitochondrial membrane 70 homolog A (S. cerevisiae)

This gene encodes an import receptor of the outer mitochondrial membrane that is part of the translocase of the outer membrane complex. This protein is involved in the import of mitochondrial precursor proteins. [provided by RefSeq, Oct 2011]

TOB1 Gene

transducer of ERBB2, 1

This gene encodes a member of the transducer of erbB-2 /B-cell translocation gene protein family. Members of this family are anti-proliferative factors that have the potential to regulate cell growth. The encoded protein may function as a tumor suppressor. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]

TOP1P1 Gene

topoisomerase (DNA) I pseudogene 1

TOP1P2 Gene

topoisomerase (DNA) I pseudogene 2

TOLLIP-AS1 Gene

TOLLIP antisense RNA 1 (head to head)

TOB2P1 Gene

transducer of ERBB2, 2 pseudogene 1

TOMM20L Gene

translocase of outer mitochondrial membrane 20 homolog (yeast)-like

TOR4A Gene

torsin family 4, member A

TOM1L1 Gene

target of myb1 (chicken)-like 1

TOP1MT Gene

topoisomerase (DNA) I, mitochondrial

This gene encodes a mitochondrial DNA topoisomerase that plays a role in the modification of DNA topology. The encoded protein is a type IB topoisomerase and catalyzes the transient breaking and rejoining of DNA to relieve tension and DNA supercoiling generated in the mitochondrial genome during replication and transcription. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]

TOLLIP Gene

toll interacting protein

This gene encodes a ubiquitin-binding protein that interacts with several Toll-like receptor (TLR) signaling cascade components. The encoded protein regulates inflammatory signaling and is involved in interleukin-1 receptor trafficking and in the turnover of IL1R-associated kinase. [provided by RefSeq, Aug 2011]

TOR3A Gene

torsin family 3, member A

TOMM34 Gene

translocase of outer mitochondrial membrane 34

The protein encoded by this gene is involved in the import of precursor proteins into mitochondria. The encoded protein has a chaperone-like activity, binding the mature portion of unfolded proteins and aiding their import into mitochondria. This protein, which is found in the cytoplasm and sometimes associated with the outer mitochondrial membrane, has a weak ATPase activity and contains 6 TPR repeats. [provided by RefSeq, Jul 2008]

TOP3A Gene

topoisomerase (DNA) III alpha

This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus reducing the number of supercoils and altering the topology of DNA. This enzyme forms a complex with BLM which functions in the regulation of recombination in somatic cells. [provided by RefSeq, Jul 2008]

TOP3B Gene

topoisomerase (DNA) III beta

This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus relaxing the supercoils and altering the topology of DNA. The enzyme interacts with DNA helicase SGS1 and plays a role in DNA recombination, cellular aging and maintenance of genome stability. Low expression of this gene may be related to higher survival rates in breast cancer patients. This gene has a pseudogene on chromosome 22. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Aug 2013]

TOX Gene

thymocyte selection-associated high mobility group box

The protein encoded by this gene contains a HMG box DNA binding domain. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. This protein may function to regulate T-cell development.[provided by RefSeq, Apr 2009]

TOM1 Gene

target of myb1 (chicken)

This gene was identified as a target of the v-myb oncogene. The encoded protein shares its N-terminal domain in common with proteins associated with vesicular trafficking at the endosome. It is recruited to the endosomes by its interaction with endofin. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]

TOPBP1 Gene

topoisomerase (DNA) II binding protein 1

This gene encodes a binding protein which interacts with the C-terminal region of topoisomerase II beta. This interaction suggests a supportive role for this protein in the catalytic reactions of topoisomerase II beta through transient breakages of DNA strands. [provided by RefSeq, Jul 2008]

TOE1 Gene

target of EGR1, member 1 (nuclear)

TOX4 Gene

TOX high mobility group box family member 4

TOX3 Gene

TOX high mobility group box family member 3

The protein encoded by this gene contains an HMG-box, indicating that it may be involved in bending and unwinding of DNA and alteration of chromatin structure. The C-terminus of the encoded protein is glutamine-rich due to CAG repeats in the coding sequence. A minor allele of this gene has been implicated in an elevated risk of breast cancer. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2009]

TOX2 Gene

TOX high mobility group box family member 2

TOR1AIP2 Gene

torsin A interacting protein 2

TOR1AIP1 Gene

torsin A interacting protein 1

This gene encodes a type 2 integral membrane protein that binds A- and B-type laminins. The encoded protein localizes to the inner nuclear membrane and may be involved in maintaining the attachment of the nuclear membrane to the nuclear lamina during cell division. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]

TOP1 Gene

topoisomerase (DNA) I

This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus altering the topology of DNA. This gene is localized to chromosome 20 and has pseudogenes which reside on chromosomes 1 and 22. [provided by RefSeq, Jul 2008]

TOMM22P1 Gene

TOMM22 pseudogene 1

TOMM22P3 Gene

TOMM22 pseudogene 3

TOMM22P5 Gene

TOMM22 pseudogene 5

TOMM22P4 Gene

TOMM22 pseudogene 4

TOMM22P6 Gene

TOMM22 pseudogene 6

TONSL Gene

tonsoku-like, DNA repair protein

The protein encoded by this gene is thought to be a negative regulator of NF-kappa-B mediated transcription. The encoded protein may bind NF-kappa-B complexes and trap them in the cytoplasm, preventing them from entering the nucleus and interacting with the DNA. Phosphorylation of this protein targets it for degradation by the ubiquitination pathway, which frees the NF-kappa-B complexes to enter the nucleus. [provided by RefSeq, Jul 2008]

TOX4P1 Gene

TOX high mobility group box family member 4 pseudogene 1

MAFD3 Gene

Major affective disorder 3, early onset

BRCA1 Gene

breast cancer 1, early onset

This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009]

BRCA2 Gene

breast cancer 2, early onset

Inherited mutations in BRCA1 and this gene, BRCA2, confer increased lifetime risk of developing breast or ovarian cancer. Both BRCA1 and BRCA2 are involved in maintenance of genome stability, specifically the homologous recombination pathway for double-strand DNA repair. The BRCA2 protein contains several copies of a 70 aa motif called the BRC motif, and these motifs mediate binding to the RAD51 recombinase which functions in DNA repair. BRCA2 is considered a tumor suppressor gene, as tumors with BRCA2 mutations generally exhibit loss of heterozygosity (LOH) of the wild-type allele. [provided by RefSeq, Dec 2008]

CCAL1 Gene

chondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis)

CTPL1 Gene

cataract, pulverulent (autosomal recessive, early-onset)

COPD Gene

Pulmonary disease, chronic obstructive, severe early-onset

BMIQ7 Gene

Obesity, susceptibility to, on chromosome 4

BMIQ10 Gene

Obesity, susceptibility to, on chromosome 10q

ASOBS Gene

Asthma and obesity susceptibility, chromosome 16p11 inversion related

AOMS1 Gene

Abdominal obesity-metabolic syndrome QTL1

AOMS2 Gene

abdominal obesity-metabolic syndrome QTL2

MEHMO Gene

mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome

FTO Gene

fat mass and obesity associated

This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA and RNA damage by oxidative demethylation. Studies in mice and humans indicate a role in nervous and cardiovascular systems and a strong association with body mass index, obesity risk, and type 2 diabetes. [provided by RefSeq, Jul 2011]

FTOP1 Gene

fat mass and obesity associated pseudogene 1

GLC1N Gene

glaucoma 1, open angle, N (juvenile-onset)

GLC1L Gene

glaucoma 1, open angle, L (adult-onset)

GLC1M Gene

glaucoma 1, open angle, M (juvenile-onset)

GLC1J Gene

glaucoma 1, open angle, J (juvenile-onset)

GLC1K Gene

glaucoma 1, open angle, K (juvenile-onset)

GLC1H Gene

glaucoma 1, open angle, H (adult-onset)

GLC1D Gene

glaucoma 1, open angle, D (adult-onset)

GLC1B Gene

glaucoma 1, open angle, B (adult-onset)

EGR2 Gene

early growth response 2

The protein encoded by this gene is a transcription factor with three tandem C2H2-type zinc fingers. Defects in this gene are associated with Charcot-Marie-Tooth disease type 1D (CMT1D), Charcot-Marie-Tooth disease type 4E (CMT4E), and with Dejerine-Sottas syndrome (DSS). Multiple transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]

EGR3 Gene

early growth response 3

This gene encodes a transcriptional regulator that belongs to the EGR family of C2H2-type zinc-finger proteins. It is an immediate-early growth response gene which is induced by mitogenic stimulation. The protein encoded by this gene participates in the transcriptional regulation of genes in controling biological rhythm. It may also play a role in a wide variety of processes including muscle development, lymphocyte development, endothelial cell growth and migration, and neuronal development. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Dec 2010]

EGR1 Gene

early growth response 1

The protein encoded by this gene belongs to the EGR family of C2H2-type zinc-finger proteins. It is a nuclear protein and functions as a transcriptional regulator. The products of target genes it activates are required for differentitation and mitogenesis. Studies suggest this is a cancer suppressor gene. [provided by RefSeq, Dec 2014]

EGR4 Gene

early growth response 4

APELA Gene

apelin receptor early endogenous ligand

EEA1 Gene

early endosome antigen 1

IER3IP1 Gene

immediate early response 3 interacting protein 1

This gene encodes a small protein that is localized to the endoplasmic reticulum (ER) and may play a role in the ER stress response by mediating cell differentiation and apoptosis. Transcription of this gene is regulated by tumor necrosis factor alpha and specificity protein 1 (Sp1). Mutations in this gene may play a role in microcephaly, epilepsy, and diabetes syndrome (MEDS), and a pseudogene of this gene is located on the long arm of chromosome 12. [provided by RefSeq, Dec 2011]

EBF4 Gene

early B-cell factor 4

EBF4 belongs to the conserved Olf/EBF family of helix-loop-helix transcription factors, members of which play important roles in neural development and B-cell maturation (Wang et al., 2002 [PubMed 12139918]).[supplied by OMIM, Mar 2008]

EBF3 Gene

early B-cell factor 3

This gene encodes a member of the early B-cell factor (EBF) family of DNA binding transcription factors. EBF proteins are involved in B-cell differentiation, bone development and neurogenesis, and may also function as tumor suppressors. The encoded protein inhibits cell survival through the regulation of genes involved in cell cycle arrest and apoptosis, and aberrant methylation or deletion of this gene may play a role in multiple malignancies including glioblastoma multiforme and gastric carcinoma. [provided by RefSeq, Sep 2011]

EBF2 Gene

early B-cell factor 2

The protein encoded by this gene belongs to the COE (Collier/Olf/EBF) family of non-basic, helix-loop-helix transcription factors that have a well conserved DNA binding domain. The COE family proteins play an important role in variety of developmental processes. Studies in mouse suggest that this gene may be involved in the differentiation of osteoblasts. [provided by RefSeq, Oct 2011]

EBF1 Gene

early B-cell factor 1

IER5L Gene

immediate early response 5-like

RAET1K Gene

retinoic acid early transcript 1K pseudogene

RAET1M Gene

retinoic acid early transcript 1M pseudogene

IER5 Gene

immediate early response 5

This gene encodes a protein that is similar to other immediate early response proteins. In the mouse, a similar gene may play an important role in mediating the cellular response to mitogenic signals. Studies in rats found the expression of a similar gene to be increased after waking and sleep deprivation. [provided by RefSeq, Jul 2008]

IER2 Gene

immediate early response 2

IER3 Gene

immediate early response 3

This gene functions in the protection of cells from Fas- or tumor necrosis factor type alpha-induced apoptosis. Partially degraded and unspliced transcripts are found after virus infection in vitro, but these transcripts are not found in vivo and do not generate a valid protein. [provided by RefSeq, Jul 2008]

MIER3 Gene

mesoderm induction early response 1, family member 3

RAET1E Gene

retinoic acid early transcript 1E

This gene belong to the RAET1 family, which consists of major histocompatibility complex (MHC) class I-related genes located in a cluster on chromosome 6q24.2-q25.3. This and RAET1G protein differ from other RAET1 proteins in that they have type I membrane-spanning sequences at their C termini rather than glycosylphosphatidylinositol anchor sequences. This protein functions as a ligand for NKG2D receptor, which is expressed on the surface of several types of immune cells, and is involved in innate and adaptive immune responses. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2011]

RAET1G Gene

retinoic acid early transcript 1G

Members of the RAET1 family, such as RAET1G, are major histocompatibility complex (MHC) class I-related genes located within a 180-kb cluster on chromosome 6q24.2-q25.3. RAET1 proteins contain MHC class I-like alpha-1 and alpha-2 domains. RAET1E (MIM 609243) and RAET1G differ from the other RAET1 proteins (e.g., RAET1I, or ULBP1; MIM 605697) in that they have type I membrane-spanning sequences at their C termini rather than glycosylphosphatidylinositol anchor sequences. (Radosavljevic et al., 2002 [PubMed 11827464]).[supplied by OMIM, Mar 2008]

RAET1F Gene

retinoic acid early transcript 1F pseudogene

RAET1L Gene

retinoic acid early transcript 1L

RAET1L belongs to the RAET1 family of major histocompatibility complex (MHC) class I-related genes, which are located within a 180-kb cluster on chromosome 6q24.2-q25.3. The REAT1 genes encode glycoproteins that contain extracellular alpha-1 and alpha-2 domains, but they lack the membrane proximal Ig-like alpha-3 domain. Most RAET1 glycoproteins are anchored to the membrane via glycosylphosphatidylinositol (GPI) linkage (Radosavljevic et al., 2002 [PubMed 11827464]).[supplied by OMIM, Mar 2008]

MIER1 Gene

mesoderm induction early response 1, transcriptional regulator

This gene encodes a protein that was first identified in Xenopus laevis by its role in a mesoderm induction early response (MIER). The encoded protein functions as a transcriptional regulator. Alternatively spliced transcript variants encode multiple isoforms, some of which lack a C-terminal nuclear localization signal. [provided by RefSeq, May 2013]

MIER2 Gene

mesoderm induction early response 1, family member 2

LOC724085 Gene

immediate early response 3 interacting protein 1 pseudogene

ASPG2 Gene

Asperger syndrome, susceptibility to, 2

ASPG3 Gene

Asperger syndrome, susceptibility to, 3

ASPG4 Gene

Asperger syndrome, susceptibility to, 4

ATOD7 Gene

Dermatitis, atopic, susceptibility to, 7

ENDO1 Gene

Endometriosis, susceptibility to, 1

HYT3 Gene

Hypertension, essential, susceptibility to, 3

HYT5 Gene

Hypertension, essential, susceptibility to, 5

HYT4 Gene

Hypertension, essential, susceptibility to, 4

HYT7 Gene

Hypertension, essential, susceptibility to, 7

HYT6 Gene

Hypertension, essential, susceptibility to, 6

HYT8 Gene

hypertension, essential, susceptibility to, 8

MGR7 Gene

Migraine with aura, susceptibility to, 7

MGR9 Gene

Migraine with aura, susceptibility to, 9

GRD2 Gene

Graves disease, susceptibility to, 2

GRDX Gene

Graves disease, susceptibility to, X-linked

EIG4 Gene

Epilepsy, idiopathic generalized, susceptibility to 4

PRAC2 Gene

prostate cancer susceptibility candidate 2

This gene is highly expressed in prostate, rectum, colon, and testis. This gene may produce a non-coding RNA or may encode a short protein that might localize to the nucleus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

PRAC1 Gene

prostate cancer susceptibility candidate 1

This gene is reported to be specifically expressed in prostate, rectum and distal colon. Sequence analysis suggests that it may play a regulatory role in the nucleus. [provided by RefSeq, Jul 2008]

SS3 Gene

Sarcoidosis, susceptibility to, 3

PSORS9 Gene

psoriasis susceptibility 9

PSORS8 Gene

psoriasis susceptibility 8

PSORS7 Gene

psoriasis susceptibility 7

PSORS6 Gene

psoriasis susceptibility 6

PSORS5 Gene

psoriasis susceptibility 5

PSORS4 Gene

psoriasis susceptibility 4

PSORS3 Gene

psoriasis susceptibility 3

NKS1 Gene

natural killer cell susceptibility 1

CELIAC8 Gene

Celiac disease, susceptibility to, 8

CELIAC5 Gene

Celiac disease, susceptibility to, 5

CELIAC6 Gene

Celiac disease, susceptibility to, 6

CELIAC7 Gene

Celiac disease, susceptibility to, 7

AIS3 Gene

autoimmune susceptibility 3 (vitiligo specific)

AIS2 Gene

autoimmune susceptibility 2

AIS1 Gene

autoimmune susceptibility 1

AIS4 Gene

autoimmune disease, susceptibility to, 4

SLEB13 Gene

Systemic lupus erythematosus, susceptibility to, 13

SLEB12 Gene

Systemic lupus erythematosus, susceptibility to, 12

SLEB15 Gene

Systemic lupus erthematosus, susceptibility to, 15

CIHL Gene

hearing loss, cisplatin-induced, susceptibility to

IGAD1 Gene

immunoglobulin A (IgA) deficiency susceptibility 1

OS4 Gene

Osteoarthritis, generalized, without dysplasia, susceptibility to

OS6 Gene

Osteoarthritis susceptibility 6

CASC4P1 Gene

cancer susceptibility candidate 4 pseudogene 1

BCC5 Gene

Basal cell carcinoma, susceptibility to, 5

NBLST5 Gene

Neuroblastoma, susceptibility to, 5

NBLST4 Gene

Neuroblastoma, susceptibility to, 4

NBLST6 Gene

Neuroblastoma, susceptibility to, 6

MAFD9 Gene

Major affective disorder-9, susceptibility to

MAFD8 Gene

Major affective disorder-8, susceptibility to

IGAN2 Gene

IgA nephropathy, susceptibility to, 2

AUTS6 Gene

Autism, susceptibility to, 6

AUTS7 Gene

Autism, susceptibility to, 7

AUTS5 Gene

Autism, susceptibility to, 5

AUTS2 Gene

autism susceptibility candidate 2

This gene has been implicated in neurodevelopment and as a candidate gene for numerous neurological disorders, including autism spectrum disorders, intellectual disability, and developmental delay. Mutations in this gene have also been associated with non-neurological disorders, such as acute lymphoblastic leukemia, aging of the skin, early-onset androgenetic alopecia, and certain cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2014]

AUTS3 Gene

Autism, susceptibility to, 3

AUTS1 Gene

Autism, susceptibility to, 1

AUTS8 Gene

Autism, susceptibility to, 8

EIG3 Gene

Epilepsy, idiopathic generalized, susceptibility to 3

EIG2 Gene

Epilepsy, idiopathic generalized, susceptibility to 2

CASC2 Gene

cancer susceptibility candidate 2 (non-protein coding)

CASC1 Gene

cancer susceptibility candidate 1

CASC6 Gene

cancer susceptibility candidate 6 (non-protein coding)

CASC5 Gene

cancer susceptibility candidate 5

The protein encoded by this gene is a component of the multiprotein assembly that is required for creation of kinetochore-microtubule attachments and chromosome segregation. The encoded protein functions as a scaffold for proteins that influence the spindle assembly checkpoint during the eukaryotic cell cycle and it interacts with at least five different kinetochore proteins and two checkpoint kinases. In adults, this gene is predominantly expressed in normal testes, various cancer cell lines and primary tumors from other tissues and is ubiquitously expressed in fetal tissues. This gene was originally identified as a fusion partner with the mixed-lineage leukemia (MLL) gene in t(11;15)(q23;q14). Mutations in this gene cause autosomal recessive primary microcephaly-4 (MCPH4). Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described but their biological validity has not been confirmed. [provided by RefSeq, Jan 2013]

CASC4 Gene

cancer susceptibility candidate 4

The increased expression level of this gene is associated with HER-2/neu proto-oncogene overexpression. Amplification and resulting overexpression of this proto-oncogene are found in approximately 30% of human breast and 20% of human ovarian cancers. Alternatively spliced variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Dec 2010]

CASC8 Gene

cancer susceptibility candidate 8 (non-protein coding)

HYT1 Gene

Hypertension, essential, susceptibility to, 1

HYT2 Gene

Hypertension, essential, susceptibility to, 2

BCC6 Gene

Basal cell carcinoma, susceptibility to, 6

CASC18 Gene

cancer susceptibility candidate 18 (non-protein coding)

ADHD2 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

CLLS1 Gene

Leukemia, chronic lymphocytic, susceptibility to, 1

LOC101930332 Gene

autism susceptibility gene 2 protein-like

ASRT8 Gene

Asthma-related traits, susceptibility to, 8

OVCAS1 Gene

Ovarian cancer, epithelial, susceptibility to

OMS Gene

otitis media, susceptibility to

EIG5 Gene

Epilepsy, idiopathic generalized, susceptibility to, 5

KAZA1 Gene

Kala-azar (visceral leishmaniasis), susceptibility to

KAZA2 Gene

Kala-azar, susceptibility to, 2

KAZA3 Gene

Kala-azar, susceptibility to, 3

DYX5 Gene

dyslexia susceptibility 5

PSORS1C1 Gene

psoriasis susceptibility 1 candidate 1

This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]

PSORS1C3 Gene

psoriasis susceptibility 1 candidate 3 (non-protein coding)

PSORS1C2 Gene

psoriasis susceptibility 1 candidate 2

AUTS11 Gene

Autism, susceptibility to, 11

AUTS12 Gene

autism, susceptibility to, 12

AUTS13 Gene

autism, susceptibility to, 13

HPC6 Gene

Prostate cancer, susceptibility to

MTBS3 Gene

Mycobacterium tuberculosis, susceptibility to, 3

MTBS2 Gene

Mycobacterium tuberculosis, susceptibility to, 2

MTBS1 Gene

mycobacterium tuberculosis, susceptibility to infection by, 1

MTBSX Gene

Mycobacterium tuberculosis, susceptibility to infection by

CASC3 Gene

cancer susceptibility candidate 3

The product of this gene is a core component of the exon junction complex (EJC), a protein complex that is deposited on spliced mRNAs at exon-exon junctions and functions in nonsense-mediated mRNA decay (NMD). The encoded protein binds RNA and interacts with two other EJC core components. It is predominantly located in the cytoplasm, but shuttles into the nucleus where it localizes to nuclear speckles. [provided by RefSeq, Jul 2008]

CASC7 Gene

cancer susceptibility candidate 7 (non-protein coding)

CASC9 Gene

cancer susceptibility candidate 9 (non-protein coding)

CHDS4 Gene

Coronary heart disease, susceptibility to, 4

CLLS3 Gene

Leukemia, chronic lymphocytic, susceptibility to, 3

CASC11 Gene

cancer susceptibility candidate 11 (non-protein coding)

CASC10 Gene

cancer susceptibility candidate 10

CASC17 Gene

cancer susceptibility candidate 17 (non-protein coding)

CASC16 Gene

cancer susceptibility candidate 16 (non-protein coding)

CASC15 Gene

cancer susceptibility candidate 15 (non-protein coding)

CASC19 Gene

cancer susceptibility candidate 19 (non-protein coding)

ADHD4 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 4

ADHD5 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 5

ADHD6 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 6

ADHD1 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 1

ADHD3 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

BULN Gene

Bulimia nervosa, susceptibility to

ALL2 Gene

Leukemia, acute lymphoblastic, susceptibility to, 2

GLM6 Gene

Glioma susceptibility 6

GLM7 Gene

Glioma susceptibility 7

GLM5 Gene

Glioma susceptibility 5

GLM8 Gene

Glioma susceptibility 8

STBMS1 Gene

Strabismus, susceptibility to, 1

IS5 Gene

scoliosis, idiopathic, susceptibility to, 5

IS4 Gene

Scoliosis, idiopathic, susceptibility to, 4

CRCS10 Gene

Colorectal cancer, susceptibility to, 10

CRCS11 Gene

Colorectal cancer, susceptibility to, 11

NPCA2 Gene

Nasopharyngeal carcinoma, susceptibility to, 2

SM2 Gene

Hepatic fibrosis susceptibility due to Schistosoma mansoni infection

SM1 Gene

Schistosoma mansoni, susceptibility/resistance to

PDCOS Gene

Podoconiosis, susceptibility to

CTEPH1 Gene

Pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to

DEL16P11.2 Gene

autism, susceptibility to, 14

BTS1 Gene

bladder tumor susceptibility 1

PTCSC1 Gene

papillary thyroid carcinoma susceptibility candidate 1 (non-protein coding)

PTCSC3 Gene

papillary thyroid carcinoma susceptibility candidate 3 (non-protein coding)

CASC23 Gene

cancer susceptibility candidate 23 (non-protein coding)

CASC22 Gene

cancer susceptibility candidate 22 (non-protein coding)

CASC20 Gene

cancer susceptibility candidate 20 (non-protein coding)

CASC21 Gene

cancer susceptibility candidate 21 (non-protein coding)

CRCS8 Gene

Colorectal cancer, susceptibility to, 8

CRCS9 Gene

colorectal cancer, susceptibility to, 9

CRCS2 Gene

Colorectal cancer, susceptibility to, 2

CRCS5 Gene

Colorectal cancer, susceptibility to, 5

MBNP Gene

?Membranous nephropathy, susceptibility to

NAFLD2 Gene

Fatty liver disease, nonalcoholic, susceptibility to, 2

ANON1 Gene

Anorexia nervosa, susceptibility to, 1

BCC4 Gene

Basal cell carcinoma, susceptibility to, 4

CMM7 Gene

Melanoma, cutaneous malignant, susceptibility to, 7

LNCR3 Gene

Lung cancer susceptibility 3

LNCR4 Gene

Lung cancer susceptibility 4

LNCR5 Gene

Lung cancer susceptibility 5

CLLS4 Gene

Leukemia, chronic lymphocytic susceptibility to, 4

AITD2 Gene

Autoimmune thyroid disease, susceptibility to, 2

AITD1 Gene

Autoimmune thyroid disease, susceptibility to, 1

AITD4 Gene

Autoimmune thyroid disease, susceptibility to, 4

ASRT6 Gene

Asthma-related traits, susceptibility to, 6

ASRT4 Gene

Asthma-related traits, susceptibility to, 4

MS3 Gene

Multiple sclerosis, susceptibility to, 3

MS2 Gene

Multiple sclerosis, susceptibility to, 2

DYX9 Gene

dyslexia susceptibility 9

DYX8 Gene

dyslexia susceptibility 8

MHS6 Gene

malignant hyperthermia susceptibility 6

MHS4 Gene

malignant hyperthermia susceptibility 4

MHS2 Gene

malignant hyperthermia susceptibility 2

MHS3 Gene

Malignant hyperthermia susceptibility 3

MGR2 Gene

Migraine, familial typical, susceptibility to

MGR3 Gene

Migraine, familial, with or without aura, susceptibility to

MGR1 Gene

Migraine with aura, susceptibility to

MGR5 Gene

Migraine with or without aura, susceptibility to, 5

MGR8 Gene

Migraine, susceptibility to, 8

TSG101 Gene

tumor susceptibility 101

The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. The gene product contains a coiled-coil domain that interacts with stathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur during breast cancer tumorigenesis and/or progression. [provided by RefSeq, Jul 2008]

HDPA Gene

Hodgkin disease, susceptibility, pseudoautosomal

ASPG1 Gene

Asperger syndrome, susceptibility to, 1

SCZD14 Gene

schizophrenia, susceptibility to, 14

SCZD11 Gene

Schizophrenia susceptibility locus, chromosome 10q-related

LOC100288160 Gene

esophagus cancer-related gene-2 interaction susceptibility protein

BCC1 Gene

Basal cell carcinoma, susceptibility to, 1

BCC2 Gene

Basal cell carcinoma, susceptibility to, 2

BCC3 Gene

Basal cell carcinoma, susceptibility to, 3

ODS1 Gene

Opioid dependence, susceptibility to, 1

PARK16 Gene

Parkinson disease 16 (susceptibility)

PARK10 Gene

Parkinson disease 10 (susceptibility)

PARK12 Gene

Parkinson disease 12 (susceptibility)

PDA1 Gene

Patent ductus arteriosus, susceptibility to

LPRS Gene

Leprosy, susceptibility to 1

CRCS6 Gene

colorectal cancer, susceptibility to, 6

MMS Gene

Malignant mesothelioma, susceptibility to

DYX1C1 Gene

dyslexia susceptibility 1 candidate 1

This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011]

MGR4 Gene

Migraine, susceptibility to, 4

HSCR9 Gene

Hirschsprung disease, susceptibility to, 9

HSCR5 Gene

Hirschsprung disease, susceptibility to, 5

The disorder described by Hirschsprung (1888) and known as Hirschsprung disease or aganglionic megacolon is characterized by congenital absence of intrinsic ganglion cells in the myenteric (Auerbach) and submucosal (Meissner) plexuses of the gastrointestinal tract. Patients are diagnosed with the short-segment form (S-HSCR, approximately 80% of cases) when the aganglionic segment does not extend beyond the upper sigmoid, and with the long-segment form (L-HSCR) when aganglionosis extends proximal to the sigmoid. Total colonic aganglionosis and total intestinal HSCR also occur (Amiel et al., 2008 [PubMed 17965226]). Isolated HSCR appears to be of complex nonmendelian inheritance with low sex-dependent penetrance and variable expression according to the length of the aganglionic segment, suggestive of the involvement of one or more genes with low penetrance (Amiel et al., 2008 [PubMed 17965226]). For a general description and a discussion of genetic heterogeneity of Hirschsprung disease (HSCR), see MIM 142623.[supplied by OMIM, Feb 2011]

PTCSC2 Gene

papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding)

DYX1 Gene

dyslexia susceptibility 1

DYX3 Gene

dyslexia susceptibility 3

DYX4 Gene

dyslexia susceptibility 4

DYX7 Gene

dyslexia susceptibility 7

DYX6 Gene

dyslexia susceptibility 6

FL1 Gene

Follicular lymphoma, susceptibility to, 1

TGCT1 Gene

testicular germ cell tumor susceptibility 1

DELXP22.11 Gene

Autism, X-linked, susceptibility to, 4

ASRT3 Gene

Asthma-related traits, susceptibility to, 3

RLS1 Gene

Restless legs syndrome, susceptibility to

RLS6 Gene

Restless legs syndrome, susceptibility to, 6

RLS5 Gene

Restless legs syndrome, susceptibility to, 5

RLS8 Gene

Restless legs syndrome, susceptibility to, 8

CELIAC9 Gene

Celiac disease, susceptibility to, 9

ALL1 Gene

Leukemia, acute lymphocytic, susceptibility to, 1

LOAS Gene

Leber optic atrophy, susceptibility to

SLEB4 Gene

systemic lupus erythematosus, susceptibility to, 4

UVM2 Gene

Melanoma, uveal, susceptibility to, 2

UVM1 Gene

Melanoma, uveal, susceptibility to, 1

ARMS2 Gene

age-related maculopathy susceptibility 2

This gene encodes a protein that is thought to play a role in diseases in the elderly. Mutations in this gene have been associated with age-related macular degeneration. [provided by RefSeq, Oct 2008]

ATHS Gene

atherosclerosis susceptibility (lipoprotein associated)

WM2 Gene

Macroglobulinemia, Waldenstrom, susceptibility to, 2

CMTS Gene

Chronic mountain sickness, susceptibility to

CHDS3 Gene

Coronary heart disease, susceptibility to, 3

CHDS2 Gene

Coronary heart disease, susceptibility to, 2

CHDS1 Gene

Coronary heart disease, susceptibility to, 1

CHDS8 Gene

Coronary heart disease, susceptibility to, 8

HHV8S Gene

Human herpesvirus 8, susceptibility to

IDDMX Gene

Diabetes mellitus, insulin-dependent, X-linked, susceptibility to

SLEB5 Gene

Systemic lupus erythematosus, susceptibility to, 5

SLEB8 Gene

Systemic lupus erythematosus, susceptibility to, 8

PSORS11 Gene

Psoriasis susceptibility 11

PSORS10 Gene

psoriasis susceptibility 10

SPDA3 Gene

Spondylarthropathy, susceptibility to, 3

SPDA2 Gene

Spondyloarthropathy, susceptibility to, 2

MGR12 Gene

Migraine, with or without aura, susceptibility to, 12

WM1 Gene

Macroglobulinemia, Waldenstrom, susceptibility to, 1

CRCS7 Gene

colorectal cancer, susceptibility to, 7

CELIAC12 Gene

Celiac disease, susceptibility to, 12

CELIAC13 Gene

Celiac disease, susceptibility to, 13

CELIAC10 Gene

Celiac disease, susceptibility to, 10

CELIAC11 Gene

Celiac disease, susceptibility to, 11

PVOP1 Gene

Pelvic organ prolapse, susceptibility to, 1

PVOP2 Gene

Pelvic organ prolapse, susceptibility to, 2

SLEB3 Gene

systemic lupus erythematosus susceptibility 3

SLEB7 Gene

Systemic lupus erythematosus, susceptibility to, 7

{obesity, early-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, early-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity (early onset extreme) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity (early onset extreme) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Obesity (early onset extreme) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Obesity (early onset extreme) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

obesity, mild, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, mild, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{osteoporosis, early-onset, susceptibility to, autosomal dominant} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {osteoporosis, early-onset, susceptibility to, autosomal dominant} phenotype from the curated OMIM Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, reducing body, X-linked, early-onset, severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 20, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sarcoidosis, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sarcoidosis, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 6, autosomal recessive early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular degeneration, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular degeneration, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Breast cancer, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Breast cancer, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, early-onset severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 6, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 6, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Recessive, Early-Onset, Pulverulent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Recessive, Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.

Sarcoidosis, Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sarcoidosis, Early-Onset from the curated CTD Gene-Disease Associations dataset.

Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset.

Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

Parkinsonism, early onset with mental retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinsonism, early onset with mental retardation from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 7, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 7, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.

early onset absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

early onset alcoholism/substance abuse. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset alcoholism/substance abuse. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrence and early onset of venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrence and early onset of venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory bowel disease (early onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel disease (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset familial alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

periodontitis, early-onset Gene Set

From GAD Gene-Disease Associations

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

early-onset prostate cancer Gene Set

From GAD Gene-Disease Associations

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

early-onset alcoholism Gene Set

From GAD Gene-Disease Associations

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

early onset of esrf in pkd1 adult polycystic kidney disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of esrf in pkd1 adult polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction (early onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, early-onset Gene Set

From GAD Gene-Disease Associations

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

familial early onset psoriasis. Gene Set

From GAD Gene-Disease Associations

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

early onset of sudden infant death. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of sudden infant death. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset ischemic heart disease. Gene Set

From GAD Gene-Disease Associations

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

early-onset aggressive diffuse amyloidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset aggressive diffuse amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia, early onset primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset periodontitis Gene Set

From GAD Gene-Disease Associations

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

early onset of multiple sclerosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypertension of early onset. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset periodontitis Gene Set

From GAD Gene-Disease Associations

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

Prostate cancer (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Prostate cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Inflammatory bowel disease (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Inflammatory bowel disease (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Myocardial infarction (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Myocardial infarction (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Breast cancer (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Breast cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

early onset of sexual maturation Gene Set

From HPO Gene-Disease Associations

genes associated with the early onset of sexual maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

macular degeneration, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular degeneration, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, early-onset, with fatal cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

breast cancer, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the breast cancer, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic failure, early onset, and neurologic disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatic failure, early onset, and neurologic disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 25, early onset, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 25, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

chondrocalcinosis with early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the chondrocalcinosis with early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 28, early onset, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 28, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

sarcoidosis, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the sarcoidosis, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{major affective disorder 3, early onset} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {major affective disorder 3, early onset} phenotype from the curated OMIM Gene-Disease Associations dataset.

osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 6, early onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 6, early onset phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset, and pituitary dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 7, autosomal recessive early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 7, autosomal recessive early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 20, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 20, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary disease, chronic obstructive, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, reducing body, x-linked, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, early-onset atypical, with myoclonic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.

adult-onset still disease; still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood-onset truncal obesity Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood-onset truncal obesity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

{obesity, late-onset} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, late-onset} phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity; obesity, morbid Gene Set

From GAD Gene-Disease Associations

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

{parkinson disease, late-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {parkinson disease, late-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease 9, late onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease 9, late onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease, late-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease, late-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease 19, late onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease 19, late onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased susceptibility to age related obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to age related obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to age related obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to age related obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

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

{obesity, susceptibility to, bmiq11} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq11} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to, bmiq8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, severe, susceptibility to, bmiq9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, severe, susceptibility to, bmiq9} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to, bmiq18} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq18} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to, bmiq4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to, bmiq12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq12} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to, bmiq10} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq10} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

{obesity, susceptibility to, bmiq7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq7} phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; obesity; energy expenditure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; obesity; energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

TOBACCO ADDICTION, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TOBACCO ADDICTION, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

{benzene toxicity, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {benzene toxicity, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{efavirenz central nervous system toxicity, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {efavirenz central nervous system toxicity, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{toxic epidermal necrolysis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {toxic epidermal necrolysis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{gilles de la tourette syndrome, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {gilles de la tourette syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioretinitis; ocular toxoplasmosis; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioretinitis; ocular toxoplasmosis; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

conjunctivitis; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease conjunctivitis; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug toxicity; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug toxicity; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular toxoplasmosis; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

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

efavirenz toxicity; nevirapine toxicity Gene Set

From GAD Gene-Disease Associations

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

epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

Primary tooth development (time to first tooth eruption) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Primary tooth development (time to first tooth eruption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Early myoclonic encephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early myoclonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

epileptic encephalopathy, early infanitle, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the epileptic encephalopathy, early infanitle, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary myopathy with early respiratory failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Galactosialidosis, early infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Galactosialidosis, early infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

early endosome lumen Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the early endosome lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

early phagosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the early phagosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

early endosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the early endosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

early endosome membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the early endosome membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

early phagosome membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the early phagosome membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

early phagosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the early phagosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

early endosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the early endosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

early endosome membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the early endosome membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

early recombination nodule Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the early recombination nodule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Epileptic Encephalopathy, Early Infantile, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.

Hereditary Myopathy with Early Respiratory Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.

early yaws Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

early myoclonic encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

early invasive cervical adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

early coronary disease. Gene Set

From GAD Gene-Disease Associations

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

humoral responses to early food allergens in children Gene Set

From GAD Gene-Disease Associations

genes associated with the disease humoral responses to early food allergens in children in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early postmenopausal bone loss at the spine. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early polyarthritis Gene Set

From GAD Gene-Disease Associations

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

temperament in early childhood Gene Set

From GAD Gene-Disease Associations

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

early cognitive decline Gene Set

From GAD Gene-Disease Associations

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

early marginal bone loss around endosseous dental implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

altered lipid oxidation and early insulin secretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease altered lipid oxidation and early insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal loss, early Gene Set

From GAD Gene-Disease Associations

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

conversion from colorectal adenoma to early carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease conversion from colorectal adenoma to early carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent early fetal loss Gene Set

From GAD Gene-Disease Associations

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

early-stage breast cancers Gene Set

From GAD Gene-Disease Associations

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

reduced early insulin response to oral glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced early insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early occlusion of coronary by-pass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early occlusion of coronary by-pass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature ovarian failure; menopause, early Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature ovarian failure; menopause, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early osteoarthritis Gene Set

From GAD Gene-Disease Associations

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

early Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein localization to early endosome Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations dataset.

early endosome to golgi transport Gene Set

From GO Biological Process Annotations

genes participating in the early endosome to golgi transport biological process from the curated GO Biological Process Annotations dataset.

protein localization to early endosome Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to early endosome biological process from the curated GO Biological Process Annotations dataset.

regulation of early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

positive regulation of early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

early endosome to recycling endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations dataset.

regulation of protein localization to early endosome Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations dataset.

positive regulation of early endosome to recycling endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations dataset.

early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

regulation of early endosome to recycling endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations dataset.

early endosome lumen Gene Set

From GO Cellular Component Annotations

proteins localized to the early endosome lumen cellular component from the curated GO Cellular Component Annotations dataset.

cytoplasmic side of early endosome membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the cytoplasmic side of early endosome membrane cellular component from the curated GO Cellular Component Annotations dataset.

early phagosome Gene Set

From GO Cellular Component Annotations

proteins localized to the early phagosome cellular component from the curated GO Cellular Component Annotations dataset.

early endosome Gene Set

From GO Cellular Component Annotations

proteins localized to the early endosome cellular component from the curated GO Cellular Component Annotations dataset.

early endosome membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the early endosome membrane cellular component from the curated GO Cellular Component Annotations dataset.

Monocyte early outgrowth colony forming units Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Monocyte early outgrowth colony forming units phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

recurrent infections in infancy and early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

early balding Gene Set

From HPO Gene-Disease Associations

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

loss of ability to walk in early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

death in early adulthood Gene Set

From HPO Gene-Disease Associations

genes associated with the death in early adulthood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Retrieval of early ER protein Rer1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retrieval of early ER protein Rer1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Radiation-inducible immediate-early gene IEX-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Radiation-inducible immediate-early gene IEX-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Immediate early response Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Immediate early response protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein LIN-9/Protein ALWAYS EARLY Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein LIN-9/Protein ALWAYS EARLY protein domain from the InterPro Predicted Protein Domain Annotations dataset.

early endosome Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the early endosome cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

early vaginal opening Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the early vaginal opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

early reproductive senescence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the early reproductive senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

early parturition Gene Set

From MPO Gene-Phenotype Associations

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

early sexual maturation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the early sexual maturation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

early eyelid opening Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the early eyelid opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

early cellular replicative senescence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the early cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

epileptic encephalopathy, early infantile, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, proximal, with early respiratory muscle involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

?epileptic encephalopathy, early infantile, 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation, developmental delay, coarse facies, and early death Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.

immediate-early-proteins Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term immediate-early-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Formation of the Early Elongation Complex Gene Set

From Reactome Pathways

proteins participating in the Formation of the Early Elongation Complex pathway from the Reactome Pathways dataset.

Phagosomal maturation (early endosomal stage) Gene Set

From Reactome Pathways

proteins participating in the Phagosomal maturation (early endosomal stage) pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the early endosome membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the early endosome membrane pathway from the Reactome Pathways dataset.

Regulation of APC/C activators between G1/S and early anaphase Gene Set

From Reactome Pathways

proteins participating in the Regulation of APC/C activators between G1/S and early anaphase pathway from the Reactome Pathways dataset.

APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set

From Reactome Pathways

proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways dataset.

Regulation of gene expression in early pancreatic precursor cells Gene Set

From Reactome Pathways

proteins participating in the Regulation of gene expression in early pancreatic precursor cells pathway from the Reactome Pathways dataset.

Early Phase of HIV Life Cycle Gene Set

From Reactome Pathways

proteins participating in the Early Phase of HIV Life Cycle pathway from the Reactome Pathways dataset.

G0 and Early G1 Gene Set

From Reactome Pathways

proteins participating in the G0 and Early G1 pathway from the Reactome Pathways dataset.

Formation of the HIV-1 Early Elongation Complex Gene Set

From Reactome Pathways

proteins participating in the Formation of the HIV-1 Early Elongation Complex pathway from the Reactome Pathways dataset.

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma, primary open angle, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma, primary open angle, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gm2-gangliosidosis, adult-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gm2-gangliosidosis, adult-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, childhood-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 19, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile-onset dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult onset ataxia with oculomotor apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult onset ataxia with oculomotor apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile-onset ascending hereditary spastic paralysis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, reducing body, X-linked, childhood-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sting-associated vasculopathy, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sting-associated vasculopathy, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, multisystem, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary open angle glaucoma juvenile onset 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary open angle glaucoma juvenile onset 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-Onset Diabetes of the Young, Type 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 7 from the curated CTD Gene-Disease Associations dataset.

Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset.

Neonatal-onset citrullinemia type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neonatal-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.

Myopathy, Distal, with Anterior Tibial Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 1 from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 2 from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 4 from the curated CTD Gene-Disease Associations dataset.

Carnitine Palmitoyltransferase II Deficiency, Late-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Late-Onset from the curated CTD Gene-Disease Associations dataset.

Hereditary spastic paralysis, infantile onset ascending Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.

MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10 from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes Of The Young, Type 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes Of The Young, Type 9 from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE, LATE-ONSET Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE, LATE-ONSET from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 3 from the curated CTD Gene-Disease Associations dataset.

Juvenile-onset dystonia Gene Set

From CTD Gene-Disease Associations

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

Albinism ocular late onset sensorineural deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Albinism ocular late onset sensorineural deafness from the curated CTD Gene-Disease Associations dataset.

Cataract, Cortical, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Cortical, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

Adult-onset citrullinemia type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adult-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.

Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type from the curated CTD Gene-Disease Associations dataset.

MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11 from the curated CTD Gene-Disease Associations dataset.

Cataract, Pulverulent, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Pulverulent, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

Late-Onset Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

variable age at onset electroclinical syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease variable age at onset electroclinical syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

maturity-onset diabetes of the young Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adult-onset still's disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult-onset still's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

variable age at onset electroclinical syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease variable age at onset electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult onset multi/minicore myopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult onset multi/minicore myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sporadic adult-onset lower motor neuron disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sporadic adult-onset lower motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory papillomatosis, juvenile-onset; recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory papillomatosis, juvenile-onset; recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

maturity onset diabetes of the young Gene Set

From GAD Gene-Disease Associations

genes associated with the disease maturity onset diabetes of the young in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menarche and menopause (age at onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarche and menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delayed onset of glycogenosis type ii. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delayed onset of glycogenosis type ii. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis (age of onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset airflow obstruction Gene Set

From GAD Gene-Disease Associations

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

menarche (age at onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarche (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

puberty onset Gene Set

From GAD Gene-Disease Associations

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

late-onset vascular disease Gene Set

From GAD Gene-Disease Associations

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

citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset airflow Gene Set

From GAD Gene-Disease Associations

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

late-onset stargardt disease Gene Set

From GAD Gene-Disease Associations

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

late onset of familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

citrullinemia, adult-onset type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease citrullinemia, adult-onset type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease (age of onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adolescent-onset antisocial behavior Gene Set

From GAD Gene-Disease Associations

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

late-onset alport syndrome Gene Set

From GAD Gene-Disease Associations

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

late onset familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late-onset congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood-onset mood disorders Gene Set

From GAD Gene-Disease Associations

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

late-onset glycogen storage disease type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late-onset glycogen storage disease type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bulbar-onset motor neuron disease Gene Set

From GAD Gene-Disease Associations

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

late-onset ad Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease (late onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease (late onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menopause (age at onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset alzheimer's disease. Gene Set

From GAD Gene-Disease Associations

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

hypertension (young onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension (young onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infantile-onset ascending hereditary spastic paralysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variable age at onset disease Gene Set

From GAD Gene-Disease Associations

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

attention deficit hyperactivity disorder (time to onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit hyperactivity disorder (time to onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma (childhood onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma (childhood onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

onset Gene Set

From GeneRIF Biological Term Annotations

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

Amyotrophic lateral sclerosis (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Alzheimer's disease (late onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Alzheimer's disease (late onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Menarche and menopause (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Menarche and menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Asthma (childhood onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Puberty onset (genital enlargement) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Puberty onset (genital enlargement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Alcohol dependence (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Menopause (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Menarche (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Femoral neck bone geometry and menarche (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bipolar disorder (age of onset and psychomotor symptoms) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bipolar disorder (age of onset and psychomotor symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Puberty onset Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Alzheimer's disease (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Alzheimer's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Puberty onset (breast development) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Puberty onset (breast development) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Narcolepsy (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Narcolepsy (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Attention deficit hyperactivity disorder (time to onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Attention deficit hyperactivity disorder (time to onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Parkinson's disease (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Parkinson's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

childhood-onset short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

childhood onset Gene Set

From HPO Gene-Disease Associations

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

late-onset distal muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the late-onset distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

middle age onset Gene Set

From HPO Gene-Disease Associations

genes associated with the middle age onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

young adult onset Gene Set

From HPO Gene-Disease Associations

genes associated with the young adult onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late-onset proximal muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the late-onset proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

developmental stagnation at onset of seizures Gene Set

From HPO Gene-Disease Associations

genes associated with the developmental stagnation at onset of seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile onset Gene Set

From HPO Gene-Disease Associations

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

insidious onset Gene Set

From HPO Gene-Disease Associations

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

late-onset spinocerebellar degeneration Gene Set

From HPO Gene-Disease Associations

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

joint swelling onset late infancy Gene Set

From HPO Gene-Disease Associations

genes associated with the joint swelling onset late infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

maturity-onset diabetes of the young Gene Set

From HPO Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late onset Gene Set

From HPO Gene-Disease Associations

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

adult onset Gene Set

From HPO Gene-Disease Associations

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

childhood onset short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

onset Gene Set

From HPO Gene-Disease Associations

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

adult-onset night blindness Gene Set

From HPO Gene-Disease Associations

genes associated with the adult-onset night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

childhood onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late onset congenital glaucoma Gene Set

From HPO Gene-Disease Associations

genes associated with the late onset congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adult onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the adult onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile onset Gene Set

From HPO Gene-Disease Associations

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

neonatal onset Gene Set

From HPO Gene-Disease Associations

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

congenital onset Gene Set

From HPO Gene-Disease Associations

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

Still's Disease, Adult-Onset Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Still's Disease, Adult-Onset phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

maturity onset diabetes of the young Gene Set

From KEGG Pathways

proteins participating in the maturity onset diabetes of the young pathway from the KEGG Pathways dataset.

late onset of menarche Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the late onset of menarche phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

glaucoma 1b, primary open angle, adult onset, Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1b, primary open angle, adult onset, phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal degeneration, late-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract with late-onset corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type viii Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type viii phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 19, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 19, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type ix Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.

cystinosis, late-onset juvenile or adolescent nephropathic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cystinosis, late-onset juvenile or adolescent nephropathic phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, kufs type, adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, kufs type, adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{bulimia nervosa, age of onset of weight loss in} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type vii Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type vii 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.

myopathy, reducing body, x-linked, childhood-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

sting-associated vasculopathy, infantile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the sting-associated vasculopathy, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, adult-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, adult-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi renotubular syndrome 4, with maturity-onset diabetes of the young Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi renotubular syndrome 4, with maturity-onset diabetes of the young phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

citrullinemia, adult-onset type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the citrullinemia, adult-onset type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease, late-onset} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease, late-onset} phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

diabetes mellitus, noninsulin-dependent, late onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the diabetes mellitus, noninsulin-dependent, late onset phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperchylomicronemia, late-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperchylomicronemia, late-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

citrullinemia, type ii, neonatal-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the citrullinemia, type ii, neonatal-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1k, primary open angle, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1k, primary open angle, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, distal, with anterior tibial onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 3a, primary open angle, congenital, juvenile, or adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3a, primary open angle, congenital, juvenile, or adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

polyarteritis nodosa, childhood-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyarteritis nodosa, childhood-onset 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.

autoimmune disease, multisystem, infantile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune disease, multisystem, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, childhood-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paralysis, infantile onset ascending Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.

Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components Gene Set

From Reactome Pathways

proteins participating in the Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components pathway from the Reactome Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

Morbid obesity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Morbid obesity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, severe, due to leptin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Morbid obesity and spermatogenic failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Abdominal obesity metabolic syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abdominal obesity metabolic syndrome from the curated CTD Gene-Disease Associations dataset.

Obesity, Abdominal Gene Set

From CTD Gene-Disease Associations

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

Obesity Gene Set

From CTD Gene-Disease Associations

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

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.

Obesity, Morbid Gene Set

From CTD Gene-Disease Associations

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

Obesity Gene Set

From dbGAP Gene-Trait Associations

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

obesity Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

obesity Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

morbid obesity Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

obesity Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypertension; inflammation; obesity; sleep apnea, obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; inflammation; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; cardiovascular diseases; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity (bmi = 30 kg/m2) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity (bmi = 30 kg/m2) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; obesity; overweight Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome x; obesity; overweight; thinness; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome x; obesity; overweight; thinness; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity-related traits Gene Set

From GAD Gene-Disease Associations

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

inflammation; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; diabetes complications; diabetes mellitus; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; diabetes complications; diabetes mellitus; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; osteoporosis Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; obesity; virilism Gene Set

From GAD Gene-Disease Associations

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

menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; hypertension; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperglycemia; obesity Gene Set

From GAD Gene-Disease Associations

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

hypertension and obesity Gene Set

From GAD Gene-Disease Associations

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

obesity; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; hypertension; obesity, localized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; obesity, localized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

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

hypercholesterolemia; obesity Gene Set

From GAD Gene-Disease Associations

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

coronary disease; obesity Gene Set

From GAD Gene-Disease Associations

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

adiposity and abdominal obesity Gene Set

From GAD Gene-Disease Associations

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

dyslipidemias; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslipidemias; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; triglycerides; diabetes, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; diabetes, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; cortisol Gene Set

From GAD Gene-Disease Associations

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

obesity; overweight; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; cholesterol, hdl; cholesterol, ldl; hypertension; lipoproteins; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; cholesterol, hdl; cholesterol, ldl; hypertension; lipoproteins; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; lipolysis Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus, type 2; hypercholesterolemia; hyperlipidemias; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus, type 2; hypercholesterolemia; hyperlipidemias; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; obesity; birth weight Gene Set

From GAD Gene-Disease Associations

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

obesity- associated hypertension ??????? Gene Set

From GAD Gene-Disease Associations

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

apnea; obesity Gene Set

From GAD Gene-Disease Associations

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

coronary disease; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; diabetes mellitus, type 2; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; glucose intolerance; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; glucose intolerance; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

endometrial neoplasms; obesity; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometrial neoplasms; obesity; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholelithiasis; obesity, morbid; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholelithiasis; obesity, morbid; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; vascular diseases Gene Set

From GAD Gene-Disease Associations

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

childhood obesity Gene Set

From GAD Gene-Disease Associations

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

hyperphagia; obesity; wagr syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperphagia; obesity; wagr syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; depression; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

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

hypertension; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

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

obesity; affective disorder Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; fatty liver; fatty liver, alcoholic; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; fatty liver; fatty liver, alcoholic; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; metabolic syndrome x; obesity, abdominal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; obesity, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; cardiovascular diseases; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity; type 2 diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; type 2 diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; cardiovascular diseases; obesity Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; obesity Gene Set

From GAD Gene-Disease Associations

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

cholesterol; triglycerides; obesity Gene Set

From GAD Gene-Disease Associations

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

body mass; insulin; lipids; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatty liver; obesity, morbid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatty liver; obesity, morbid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; dyslipidemias; hypertension; metabolic syndrome x; obesity; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; dyslipidemias; hypertension; metabolic syndrome x; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-2-macroglobulin concentration obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-2-macroglobulin concentration obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity, localized Gene Set

From GAD Gene-Disease Associations

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

head and neck neoplasms; kidney neoplasms; lung neoplasms; neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head and neck neoplasms; kidney neoplasms; lung neoplasms; neoplasms; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; psoriasis Gene Set

From GAD Gene-Disease Associations

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

obesity; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hypertension; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; body weight Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity; bone mineral density Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity; hypertension Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hyperlipidemia; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hyperlipidemia; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; retinal vascular occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; retinal vascular occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; obesity Gene Set

From GAD Gene-Disease Associations

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

triglycerides; insulin; obesity Gene Set

From GAD Gene-Disease Associations

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

hyperlipidemias; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; ischemic attack, transient; obesity; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; ischemic attack, transient; obesity; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; obesity; glucose; leptin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; obesity; glucose; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; insulin resistance; obesity; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; insulin resistance; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; obesity Gene Set

From GAD Gene-Disease Associations

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

dyslipidemias; obesity Gene Set

From GAD Gene-Disease Associations

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

body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

obesity; postthrombotic syndrome; varicose veins; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; postthrombotic syndrome; varicose veins; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity and insulin response Gene Set

From GAD Gene-Disease Associations

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

obesity; overnutrition; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; overnutrition; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; obesity; leptin Gene Set

From GAD Gene-Disease Associations

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

hemochromatosis; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; overweight Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus. obesity. and lipaemia Gene Set

From GAD Gene-Disease Associations

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

obesity; prostate cancer Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; obesity, morbid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; obesity, morbid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperinsulinism; hyperphagia; obesity Gene Set

From GAD Gene-Disease Associations

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

coronary stenosis; hypercholesterolemia; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary stenosis; hypercholesterolemia; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity ; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

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

angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatty liver; hepatitis; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatty liver; hepatitis; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; blood pressure, arterial; sleep apnea Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; blood pressure, arterial; sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; insulin; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; stroke Gene Set

From GAD Gene-Disease Associations

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

obesity and type 2 diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity and type 2 diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; obesity Gene Set

From GAD Gene-Disease Associations

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

fatty liver; liver cirrhosis; obesity, morbid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatty liver; liver cirrhosis; obesity, morbid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; obesity; rectal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic neoplasms; obesity; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity ????????? Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome x; obesity, morbid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome x; obesity, morbid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; insulin; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity, morbid; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; diabetes Gene Set

From GAD Gene-Disease Associations

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

myocardial infarct; lipoprotein; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; lipoprotein; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; obesity; glucose; leptin; cortisol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; obesity; glucose; leptin; cortisol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome x; obesity, abdominal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome x; obesity, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; myocardial infarction; obesity; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; myocardial infarction; obesity; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; obesity; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; obesity; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; ovarian cancer Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 2; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; obesity; osteoarthritis, knee; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; obesity; osteoarthritis, knee; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cardiovascular diseases; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cardiovascular diseases; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; metabolic syndrome x; obesity 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.

insulin resistance; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyslipidemias; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslipidemias; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism disorders; obesity Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; obesity Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, morbid Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 2; glucose intolerance; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperglycemia; insulin resistance; myocardial infarction; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperglycemia; insulin resistance; myocardial infarction; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity and osteoporosis Gene Set

From GAD Gene-Disease Associations

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

acanthosis nigricans; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acanthosis nigricans; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperinsulinism; hypertriglyceridemia; obesity Gene Set

From GAD Gene-Disease Associations

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

lipids; obesity; glucose; cortisol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; obesity; glucose; cortisol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; neoplasms; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; neoplasms; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; obesity Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; diabetes complications; diabetes mellitus; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes complications; diabetes mellitus; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma; obesity, localized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma; obesity, localized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; metabolic syndrome x; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; smoking behavior; obesity, localized; memory disturbance; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; smoking behavior; obesity, localized; memory disturbance; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance in obesity Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperlipidemias; myocardial infarction; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperlipidemias; myocardial infarction; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; breast cancer Gene Set

From GAD Gene-Disease Associations

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

body weight; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; diabetes mellitus; dyslipidemias; hypertension; obesity; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus; dyslipidemias; hypertension; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; c-reactive protein; obesity; glucose; leptin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; c-reactive protein; obesity; glucose; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; metabolic diseases; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; insulin; lipids; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; insulin; lipids; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intrauterine growth; obesity; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intrauterine growth; obesity; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus; obesity Gene Set

From GAD Gene-Disease Associations

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

obesity and glucose homeostasis Gene Set

From GAD Gene-Disease Associations

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

obesity; bulimia nervosa Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; hyperandrogenism Gene Set

From GAD Gene-Disease Associations

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

obesity; polycystic ovarian syndrome; hyperandrogenism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; polycystic ovarian syndrome; hyperandrogenism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; sleep apnea, obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes complications; hypercholesterolemia; hypertension; myocardial infarction; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; hypercholesterolemia; hypertension; myocardial infarction; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; obesity; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; obesity; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; insulin; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acanthosis nigricans; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 2; hypertriglyceridemia; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; hypertriglyceridemia; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disease models, animal; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disease models, animal; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; asthma Gene Set

From GAD Gene-Disease Associations

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

obesity (extreme) Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus, type 2; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperphagia; obesity Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; obesity Gene Set

From GAD Gene-Disease Associations

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

endometrial neoplasms; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometrial neoplasms; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; hyperlipidemias; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; hyperlipidemias; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; cardiovascular disease; obesity; hyperuricemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; cardiovascular disease; obesity; hyperuricemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; obesity; syndrome Gene Set

From GAD Gene-Disease Associations

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

dyslipidemias; metabolic syndrome x; obesity; renal hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslipidemias; metabolic syndrome x; obesity; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; weight gain Gene Set

From GAD Gene-Disease Associations

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

cellulitis; obesity Gene Set

From GAD Gene-Disease Associations

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

hypertension; obesity Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyslipidemias; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslipidemias; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, abdominal; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, abdominal; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, morbid; postoperative complications; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; postoperative complications; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; obesity; adiponectin Gene Set

From GAD Gene-Disease Associations

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

obesity; bmi Gene Set

From GAD Gene-Disease Associations

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

fatty liver; obesity Gene Set

From GAD Gene-Disease Associations

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