Name

non-syndromic intellectual disability Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Syndromic intellectual disability Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

syndromic intellectual disability Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

syndromic intellectual disability Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Blepharophimosis-ptosis-intellectual disability syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coffin Siris/Intellectual Disability Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coffin Siris/Intellectual Disability phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intellectual Disability Gene Set

From CTD Gene-Disease Associations

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

intellectual disability Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

intellectual disability Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intellectual disability, moderate Gene Set

From HPO Gene-Disease Associations

genes associated with the intellectual disability, moderate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intellectual disability, severe Gene Set

From HPO Gene-Disease Associations

genes associated with the intellectual disability, severe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intellectual disability, progressive Gene Set

From HPO Gene-Disease Associations

genes associated with the intellectual disability, progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intellectual disability, profound Gene Set

From HPO Gene-Disease Associations

genes associated with the intellectual disability, profound phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intellectual disability, mild Gene Set

From HPO Gene-Disease Associations

genes associated with the intellectual disability, mild phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intellectual disability Gene Set

From HPO Gene-Disease Associations

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

Intellectual Disability Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

blepharophimosis-ptosis-intellectual disability syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

non-syndromic x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-syndromic x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Non-syndromic genetic deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Non-syndromic genetic deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

non-syndromic cleft lip and palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-syndromic cleft lip and palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-syndromic neurosensory deafness (dfnb1) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-syndromic neurosensory deafness (dfnb1) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-syndromic deafness Gene Set

From GAD Gene-Disease Associations

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

non-syndromic cleft lip Gene Set

From GAD Gene-Disease Associations

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

dominant non-syndromic sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dominant non-syndromic sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-syndromic oligodontia Gene Set

From GAD Gene-Disease Associations

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

X-linked mental retardation, syndromic, Claes-Jensen type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic, Claes-Jensen type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, turner type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, turner type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked syndromic 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked syndromic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndromic X-linked mental retardation 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndromic X-linked mental retardation 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, raymond type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, raymond type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, syndromic 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 32 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, wu type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, wu type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, Hedera type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, Hedera type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked syndromic mental retardation, Nascimento type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked syndromic mental retardation, Nascimento type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental Retardation, X-Linked, Syndromic 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 13 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 12 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 14 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE from the curated CTD Gene-Disease Associations dataset.

Mental retardation X-linked syndromic 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation X-linked syndromic 7 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Jarid1c-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Jarid1c-Related from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Christianson Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Christianson Type from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, syndromic 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, syndromic 5 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Turner Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Turner Type from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 10 from the curated CTD Gene-Disease Associations dataset.

?mental retardation, x-linked syndromic 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked syndromic 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic, hedera type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic, hedera type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, shashi type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, shashi type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, claes-jensen type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, claes-jensen type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, nascimento-type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, nascimento-type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 15 (cabezas type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 15 (cabezas type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, chudley-schwartz type, Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, chudley-schwartz type, phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, raymond type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, raymond type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, abidi type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, abidi type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, turner type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, turner type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, lubs type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, lubs type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, christianson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, christianson type phenotype from the curated OMIM Gene-Disease Associations dataset.

burkitt lymphoma; hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoproliferative disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease burkitt lymphoma; hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoma, t-cell; t-cell lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoma, t-cell; t-cell lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, non-hodgkin; lymphoma, non-hodgkin's; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, non-hodgkin; lymphoma, non-hodgkin's; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brill-symmers disease; lymphoma, follicular; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

b-cell lymphomas; lymphoma, b-cell; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease b-cell lymphomas; lymphoma, b-cell; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

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

leukemia; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

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

non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Deafness, cochlear, with myopia and intellectual impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

intellectual Gene Set

From GeneRIF Biological Term Annotations

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

non-specific x-linked mental retardation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-specific x-linked mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

learning disability Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

learning disability Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

attention deficit hyperactivity disorder; reading disability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit hyperactivity disorder; reading disability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disability Gene Set

From GeneRIF Biological Term Annotations

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

Relative hand skill in reading disability Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

learning disability Gene Set

From GWASdb SNP-Disease Associations

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

specific learning disability Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the specific learning disability phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

specific learning disability Gene Set

From HPO Gene-Disease Associations

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

Microphthalmia syndromic 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia syndromic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diarrhea 3, secretory sodium, congenital, syndromic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia syndromic 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia syndromic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia syndromic 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia syndromic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, syndromic, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, syndromic, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, syndromic 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, syndromic 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, syndromic 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, syndromic 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, syndromic multisystem Gene Set

From ClinVar Gene-Phenotype Associations

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

Microphthalmia, syndromic 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, syndromic 2 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, syndromic 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, syndromic 1 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, syndromic 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, syndromic 7 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Syndromic 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Syndromic 5 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Syndromic 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Syndromic 4 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Syndromic 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Syndromic 6 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Syndromic 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Syndromic 3 from the curated CTD Gene-Disease Associations dataset.

syndromic Gene Set

From GeneRIF Biological Term Annotations

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

syndromic hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the syndromic hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

syndromic hearing impairment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the syndromic hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

?microphthalmia, syndromic 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microphthalmia, syndromic 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

?microphthalmia, syndromic 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microphthalmia, syndromic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

diarrhea 3, secretory sodium, congenital, syndromic Gene Set

From OMIM Gene-Disease Associations

genes associated with the diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 11, syndromic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 11, syndromic phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, syndromic 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, syndromic 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

dorsolateral (non-cerebellar) part of isA Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in dorsolateral (non-cerebellar) part of isA relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Non-small cell lung cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Non-small cell lung cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Non-ketotic hyperglycinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Non-ketotic hyperglycinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

non-membrane-bounded organelle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the non-membrane-bounded organelle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intracellular non-membrane-bounded organelle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intracellular non-membrane-bounded organelle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intracellular non-membrane-bounded organelle Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the intracellular non-membrane-bounded organelle cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

non-membrane-bounded organelle Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the non-membrane-bounded organelle cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

extracellular non-membrane-bounded organelle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

non-membrane-bounded organelle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

non-growing cell tip Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the non-growing cell tip cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

intracellular non-membrane-bounded organelle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

9S-cytosolic aryl hydrocarbon (Ah) receptor non-ligand activated complex Gene Set

From CORUM Protein Complexes

proteins in the 9S-cytosolic aryl hydrocarbon (Ah) receptor non-ligand activated complex protein complex from the CORUM Protein Complexes dataset.

3,4,5-trihydroxy-2--methoxy-8,8-dimethyl-N-(hexahydro-2-oxo-6-(cyclohexylcarbonyl)oxy-2H-azepin-3-yl)non-6-enamide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 3,4,5-trihydroxy-2--methoxy-8,8-dimethyl-N-(hexahydro-2-oxo-6-(cyclohexylcarbonyl)oxy-2H-azepin-3-yl)non-6-enamide from the curated CTD Gene-Chemical Interactions dataset.

Anti-Inflammatory Agents, Non-Steroidal Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Anti-Inflammatory Agents, Non-Steroidal from the curated CTD Gene-Chemical Interactions dataset.

Non-alcoholic Fatty Liver Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Non-alcoholic Fatty Liver Disease from the curated CTD Gene-Disease Associations dataset.

Carcinoma, Non-Small-Cell Lung Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carcinoma, Non-Small-Cell Lung from the curated CTD Gene-Disease Associations dataset.

Lymphoma, Non-Hodgkin Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lymphoma, Non-Hodgkin from the curated CTD Gene-Disease Associations dataset.

Epidermolysis Bullosa, Junctional, Non-Herlitz Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis Bullosa, Junctional, Non-Herlitz Type from the curated CTD Gene-Disease Associations dataset.

Non-alcoholic Fatty Liver Disease [Supplementary Concept] Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Non-alcoholic Fatty Liver Disease [Supplementary Concept] in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Carcinoma, Non-Small-Cell Lung Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Carcinoma, Non-Small-Cell Lung in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

non-langerhans-cell histiocytosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease non-langerhans-cell histiocytosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

non-small cell lung carcinoma Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease non-small cell lung carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

non-hodgkin lymphoma Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

non-invasive bladder papillary urothelial neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-invasive bladder papillary urothelial neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

non-secretory myeloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

testicular non-seminomatous germ cell cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

non-langerhans-cell histiocytosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central nervous system mesenchymal non-meningothelial tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

non-gestational choriocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

non-functioning pancreatic endocrine tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-functioning pancreatic endocrine tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

non-hodgkin lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

non-small cell lung carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-small cell lung carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

testicular germ cell tumor non-seminomatous Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease testicular germ cell tumor non-seminomatous in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

non-suppurative otitis media Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

non-gestational ovarian choriocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

non-proliferative fibrocystic change of the breast Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-proliferative fibrocystic change of the breast in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

4-[(1S,2S,5S,9R)-5-(HYDROXYMETHYL)-8,9-DIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-[(1S,2S,5S,9R)-5-(HYDROXYMETHYL)-8,9-DIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL drug from the curated DrugBank Drug Targets dataset.

(E)-(2r,3r,4s,5r)-3,4,5-Trihydroxy-2-Methoxy-8,8-Dimethyl-Non-6-Enoic Acid ((3s,6r)-6-Hydroxy-2-Oxo-Azepan-3-Yl)-Amide Gene Set

From DrugBank Drug Targets

interacting proteins for the (E)-(2r,3r,4s,5r)-3,4,5-Trihydroxy-2-Methoxy-8,8-Dimethyl-Non-6-Enoic Acid ((3s,6r)-6-Hydroxy-2-Oxo-Azepan-3-Yl)-Amide drug from the curated DrugBank Drug Targets dataset.

4-[(1S,2S,5S)-5-(HYDROXYMETHYL)-8-METHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-[(1S,2S,5S)-5-(HYDROXYMETHYL)-8-METHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL drug from the curated DrugBank Drug Targets dataset.

4-[(1S,2S,5S)-5-(HYDROXYMETHYL)-6,8,9-TRIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-[(1S,2S,5S)-5-(HYDROXYMETHYL)-6,8,9-TRIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL drug from the curated DrugBank Drug Targets dataset.

4-[(1S,2R,5S)-4,4,8-TRIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-[(1S,2R,5S)-4,4,8-TRIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL drug from the curated DrugBank Drug Targets dataset.

non-st-elevation acute coronary syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-st-elevation acute coronary syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease in non-type 1 diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease in non-type 1 diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma; non-hodgkin's lymphoma Gene Set

From GAD Gene-Disease Associations

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

high insulin concentrations in non-diabetic mexican ameri Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high insulin concentrations in non-diabetic mexican ameri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; exanthema; lung neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; exanthema; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-secretor status Gene Set

From GAD Gene-Disease Associations

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

lymphoma, b-cell; lymphoma, non-hodgkin; lymphoma, t-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, b-cell; lymphoma, non-hodgkin; lymphoma, t-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-hodgkin lymphoma Gene Set

From GAD Gene-Disease Associations

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

childhood b-cell non-hodgkin's lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease childhood b-cell non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-papillary renal cell carcinomas Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-papillary renal cell carcinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; breast neoplasms; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; breast neoplasms; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; lung neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

two major non-ribosomal nucleolar proteins and its implication Gene Set

From GAD Gene-Disease Associations

genes associated with the disease two major non-ribosomal nucleolar proteins and its implication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-hodgkin lymphomas Gene Set

From GAD Gene-Disease Associations

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

lung cancer; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-small-cell lung cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-small-cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, hepatocellular; liver neoplasms; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, hepatocellular; liver neoplasms; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

b- and t-cell non-hodgkin's lymphomas Gene Set

From GAD Gene-Disease Associations

genes associated with the disease b- and t-cell non-hodgkin's lymphomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, chronic, b-cell; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, chronic, b-cell; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lactase non-persistence Gene Set

From GAD Gene-Disease Associations

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

non-hodgkin's lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, large b-cell, diffuse; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-type 1 diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-type 1 diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-hodgkin's b cell lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-hodgkin's b cell lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-smokers. Gene Set

From GAD Gene-Disease Associations

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

adenocarcinoma; carcinoma, non-small-cell lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-small cell lung carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c, chronic; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c, chronic; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

red vs non-red hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red vs non-red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, large b-cell, diffuse; lymphoma, non-hodgkin; lymphoma, t-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, non-hodgkin; lymphoma, t-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, b-cell; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, b-cell; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary non-polyposis colon cancer. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary non-polyposis colon cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma fibrinogen levels in smokers and non-smokers Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma fibrinogen levels in smokers and non-smokers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-allergic nasal polyposis Gene Set

From GAD Gene-Disease Associations

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

cardiovascular events in non-smokers Gene Set

From GAD Gene-Disease Associations

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

hepatitis, fulminant non-a, nonb Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis, fulminant non-a, nonb in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-inflammatory breast carcinomas Gene Set

From GAD Gene-Disease Associations

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

non-small cell lung cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-small cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

steatohepatitis, non-alcoholic Gene Set

From GAD Gene-Disease Associations

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

adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosomal instability; immunologic deficiency syndromes; lymphoma, non-hodgkin; microsatellite instability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosomal instability; immunologic deficiency syndromes; lymphoma, non-hodgkin; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic non-spherocytic haemolytic anaemia. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic non-spherocytic haemolytic anaemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin disease; lymphoma; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

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

carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, non-hodgkin; neoplasm invasiveness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, non-hodgkin; neoplasm invasiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease in non-insulin-dependent diabetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease in non-insulin-dependent diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin disease; lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

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

t-cell non-hodgkin's lymphomas Gene Set

From GAD Gene-Disease Associations

genes associated with the disease t-cell non-hodgkin's lymphomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; myocardial dysfunction, non-ischaemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, coronary; myocardial dysfunction, non-ischaemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin's disease; non-hodgkin's lymphoma Gene Set

From GAD Gene-Disease Associations

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

familial non-ret c cell hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial non-ret c cell hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, non-hodgkin Gene Set

From GAD Gene-Disease Associations

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

non-alcoholic fatty liver disease Gene Set

From GAD Gene-Disease Associations

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

adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non Gene Set

From GeneRIF Biological Term Annotations

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

PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

positive regulation of non-canonical wnt signaling pathway via jnk cascade Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of non-canonical wnt signaling pathway via jnk cascade biological process from the curated GO Biological Process Annotations dataset.

pentose-phosphate shunt, non-oxidative branch Gene Set

From GO Biological Process Annotations

genes participating in the pentose-phosphate shunt, non-oxidative branch biological process from the curated GO Biological Process Annotations dataset.

regulation of chronic inflammatory response to non-antigenic stimulus Gene Set

From GO Biological Process Annotations

genes participating in the regulation of chronic inflammatory response to non-antigenic stimulus biological process from the curated GO Biological Process Annotations dataset.

positive regulation of non-canonical wnt signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of non-canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of acute inflammatory response to non-antigenic stimulus Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of acute inflammatory response to non-antigenic stimulus biological process from the curated GO Biological Process Annotations dataset.

non-canonical wnt signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the non-canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of non-canonical wnt signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of non-canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations dataset.

non-canonical wnt signaling pathway via jnk cascade Gene Set

From GO Biological Process Annotations

genes participating in the non-canonical wnt signaling pathway via jnk cascade biological process from the curated GO Biological Process Annotations dataset.

negative regulation of circadian sleep/wake cycle, non-rem sleep Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations dataset.

regulation of vacuole fusion, non-autophagic Gene Set

From GO Biological Process Annotations

genes participating in the regulation of vacuole fusion, non-autophagic biological process from the curated GO Biological Process Annotations dataset.

circadian sleep/wake cycle, non-rem sleep Gene Set

From GO Biological Process Annotations

genes participating in the circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations dataset.

regulation of non-canonical wnt signaling pathway via jnk cascade Gene Set

From GO Biological Process Annotations

genes participating in the regulation of non-canonical wnt signaling pathway via jnk cascade biological process from the curated GO Biological Process Annotations dataset.

nuclear-transcribed mrna catabolic process, non-stop decay Gene Set

From GO Biological Process Annotations

genes participating in the nuclear-transcribed mrna catabolic process, non-stop decay biological process from the curated GO Biological Process Annotations dataset.

positive regulation of chronic inflammatory response to non-antigenic stimulus Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of chronic inflammatory response to non-antigenic stimulus biological process from the curated GO Biological Process Annotations dataset.

regulation of circadian sleep/wake cycle, non-rem sleep Gene Set

From GO Biological Process Annotations

genes participating in the regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations dataset.

regulation of non-canonical wnt signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of non-canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations dataset.

vacuole fusion, non-autophagic Gene Set

From GO Biological Process Annotations

genes participating in the vacuole fusion, non-autophagic biological process from the curated GO Biological Process Annotations dataset.

non-recombinational repair Gene Set

From GO Biological Process Annotations

genes participating in the non-recombinational repair biological process from the curated GO Biological Process Annotations dataset.

regulation of acute inflammatory response to non-antigenic stimulus Gene Set

From GO Biological Process Annotations

genes participating in the regulation of acute inflammatory response to non-antigenic stimulus biological process from the curated GO Biological Process Annotations dataset.

protection from non-homologous end joining at telomere Gene Set

From GO Biological Process Annotations

genes participating in the protection from non-homologous end joining at telomere biological process from the curated GO Biological Process Annotations dataset.

positive regulation of circadian sleep/wake cycle, non-rem sleep Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations dataset.

non-canonical wnt signaling pathway involved in heart development Gene Set

From GO Biological Process Annotations

genes participating in the non-canonical wnt signaling pathway involved in heart development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of acute inflammatory response to non-antigenic stimulus Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of acute inflammatory response to non-antigenic stimulus biological process from the curated GO Biological Process Annotations dataset.

non-canonical wnt signaling pathway via mapk cascade Gene Set

From GO Biological Process Annotations

genes participating in the non-canonical wnt signaling pathway via mapk cascade biological process from the curated GO Biological Process Annotations dataset.

non-membrane-bounded organelle Gene Set

From GO Cellular Component Annotations

proteins localized to the non-membrane-bounded organelle cellular component from the curated GO Cellular Component Annotations dataset.

intracellular non-membrane-bounded organelle Gene Set

From GO Cellular Component Annotations

proteins localized to the intracellular non-membrane-bounded organelle cellular component from the curated GO Cellular Component Annotations dataset.

neurotensin receptor activity, non-g-protein coupled Gene Set

From GO Molecular Function Annotations

genes performing the neurotensin receptor activity, non-g-protein coupled molecular function from the curated GO Molecular Function Annotations dataset.

translation factor activity, non-nucleic acid binding Gene Set

From GO Molecular Function Annotations

genes performing the translation factor activity, non-nucleic acid binding molecular function from the curated GO Molecular Function Annotations dataset.

non-membrane spanning protein tyrosine kinase activity Gene Set

From GO Molecular Function Annotations

genes performing the non-membrane spanning protein tyrosine kinase activity molecular function from the curated GO Molecular Function Annotations dataset.

non-membrane spanning protein tyrosine phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the non-membrane spanning protein tyrosine phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

[35S]non-peptide OT antagonist Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [35S]non-peptide OT antagonist ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Response to irinotecan in non-small-cell lung cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to irinotecan in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Acute urticaria and angioedema (non-steroidal anti-inflammatory drug-induced) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Acute urticaria and angioedema (non-steroidal anti-inflammatory drug-induced) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Red vs non-red hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-small cell lung cancer (survival) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-small cell lung cancer (survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-word repetition Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-word repetition phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-alcoholic fatty liver disease histology (other) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-alcoholic fatty liver disease histology (other) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-alcoholic fatty liver disease histology (lobular) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-alcoholic fatty liver disease histology (lobular) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-small cell lung cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-small cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-albumin protein levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-albumin protein levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-substance related behavioral disinhibition Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-substance related behavioral disinhibition phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Vitiligo (non-segmental) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Vitiligo (non-segmental) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-obstructive azoospermia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-obstructive azoospermia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Body mass index (non-asthmatics) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Body mass index (non-asthmatics) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to platinum-based chemotherapy in non-small-cell lung cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-alcoholic fatty liver disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Retinopathy in non-diabetics Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Retinopathy in non-diabetics phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-melanoma skin cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-melanoma skin cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

non-small cell lung carcinoma Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

non-hodgkin lymphoma Gene Set

From GWASdb SNP-Disease Associations

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

non-obstructive azoospermia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the non-obstructive azoospermia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

non-hodgkin lymphoma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the non-hodgkin lymphoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

non-caseating epithelioid cell granulomatosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the non-caseating epithelioid cell granulomatosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

non-midline cleft lip Gene Set

From HPO Gene-Disease Associations

genes associated with the non-midline cleft lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

non-hodgkin lymphoma Gene Set

From HPO Gene-Disease Associations

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

non-caseating epithelioid cell granulomatosis Gene Set

From HPO Gene-Disease Associations

genes associated with the non-caseating epithelioid cell granulomatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

non-midline cleft palate Gene Set

From HPO Gene-Disease Associations

genes associated with the non-midline cleft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

non-acidotic proximal tubulopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the non-acidotic proximal tubulopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated tissue non-specific alkaline phosphatase Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated tissue non-specific alkaline phosphatase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin fragility with non-scarring blistering Gene Set

From HPO Gene-Disease Associations

genes associated with the skin fragility with non-scarring blistering phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atypical nevi in non-sun exposed areas Gene Set

From HPO Gene-Disease Associations

genes associated with the atypical nevi in non-sun exposed areas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Carcinoma, Non-Small-Cell Lung Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Carcinoma, Non-Small-Cell Lung phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lymphoma, Non-Hodgkin Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

pentose phosphate pathway (non-oxidative branch) Gene Set

From HumanCyc Pathways

proteins participating in the pentose phosphate pathway (non-oxidative branch) pathway from the HumanCyc Pathways dataset.

Non-structural maintenance of chromosome element 4, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Non-structural maintenance of chromosome element 4, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, non-receptor type-3, -4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, non-receptor type-3, -4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, non-receptor type-6, -11 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, non-receptor type-6, -11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, non-receptor type-1/2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, non-receptor type-1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Non-canonical purine NTP phosphatase/PRRC1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Non-canonical purine NTP phosphatase/PRRC1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

26S proteasome regulatory complex, non-ATPase subcomplex, Rpn1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 26S proteasome regulatory complex, non-ATPase subcomplex, Rpn1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

26S proteasome non-ATPase regulatory subunit 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 26S proteasome non-ATPase regulatory subunit 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, receptor/non-receptor type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, receptor/non-receptor type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Globular protein, non-globular alpha/beta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Globular protein, non-globular alpha/beta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Non-receptor tyrosine-protein phosphatase 22 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Non-receptor tyrosine-protein phosphatase 22 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/RNA non-specific endonuclease, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/RNA non-specific endonuclease, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein phosphatase non-receptor type 23 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein phosphatase non-receptor type 23 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, non-receptor type-12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, non-receptor type-12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, non-receptor, TYK2, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, non-receptor, TYK2, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

N-acetyltransferase B complex, non-catalytic subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the N-acetyltransferase B complex, non-catalytic subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14, caspase non-catalytic subunit p10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14, caspase non-catalytic subunit p10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, non-receptor SYK/ZAP-70 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, non-receptor SYK/ZAP-70 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Netrin module, non-TIMP type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Netrin module, non-TIMP type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

26S proteasome non-ATPase regulatory subunit Rpn12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 26S proteasome non-ATPase regulatory subunit Rpn12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, non-receptor Jak/Tyk2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, non-receptor Jak/Tyk2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, non-receptor type-14, -21 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, non-receptor type-14, -21 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sigma non-opioid intracellular receptor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sigma non-opioid intracellular receptor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/RNA non-specific endonuclease Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/RNA non-specific endonuclease protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, non-receptor Jak2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, non-receptor Jak2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, non-receptor Jak3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, non-receptor Jak3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, non-receptor Jak1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, non-receptor Jak1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Non-structural maintenance of chromosomes element 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Non-structural maintenance of chromosomes element 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sodium leak channel non-selective protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sodium leak channel non-selective protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein phosphatase non-receptor type 13 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein phosphatase non-receptor type 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Non-SMC condensin II complex, subunit H2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Non-SMC condensin II complex, subunit H2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit, Trm82 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit, Trm82 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

26S proteasome regulatory complex, non-ATPase subcomplex, Rpn2/Psmd1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 26S proteasome regulatory complex, non-ATPase subcomplex, Rpn2/Psmd1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Collagen IV, non-collagenous Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Collagen IV, non-collagenous protein domain from the InterPro Predicted Protein Domain Annotations dataset.

non small cell lung cancer Gene Set

From KEGG Pathways

proteins participating in the non small cell lung cancer pathway from the KEGG Pathways dataset.

intracellular non-membrane-bounded organelle Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the intracellular non-membrane-bounded organelle cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

non-membrane-bounded organelle Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the non-membrane-bounded organelle cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

abnormal non-rapid eye movement sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

non-obstructive hydrocephaly Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the non-obstructive hydrocephaly phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

non-pigmented tail tip Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the non-pigmented tail tip phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased lung non-small cell carcinoma incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased lung non-small cell carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating non-hdl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating non-hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

epidermolysis bullosa, junctional, non-herlitz type Gene Set

From OMIM Gene-Disease Associations

genes associated with the epidermolysis bullosa, junctional, non-herlitz type phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphoma, non-hodgkin, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphoma, non-hodgkin, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

{diabetes mellitus, non-insulin-dependent, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {diabetes mellitus, non-insulin-dependent, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphoma, non-hodgkin Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphoma, non-hodgkin phenotype from the curated OMIM Gene-Disease Associations dataset.

[hyperphenylalaninemia, non-pku mild] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [hyperphenylalaninemia, non-pku mild] phenotype from the curated OMIM Gene-Disease Associations dataset.

b-cell non-hodgkin lymphoma, high-grade Gene Set

From OMIM Gene-Disease Associations

genes associated with the b-cell non-hodgkin lymphoma, high-grade phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphoma, b-cell non-hodgkin, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphoma, b-cell non-hodgkin, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

non-hodgkin lymphoma, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the non-hodgkin lymphoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

Class IB PI3K non-lipid kinase events Gene Set

From PID Pathways

proteins participating in the Class IB PI3K non-lipid kinase events pathway from the PID Pathways dataset.

non-small cell lung cancer cell line Gene Set

From ProteomicsDB Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in non-small cell lung cancer cell line relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset.

Non-integrin membrane-ECM interactions Gene Set

From Reactome Pathways

proteins participating in the Non-integrin membrane-ECM interactions pathway from the Reactome Pathways dataset.

Metabolism of non-coding RNA Gene Set

From Reactome Pathways

proteins participating in the Metabolism of non-coding RNA pathway from the Reactome Pathways dataset.

Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell Gene Set

From Reactome Pathways

proteins participating in the Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell pathway from the Reactome Pathways dataset.

non-small cell lung cancer cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue non-small cell lung cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

non-small cell lung cancer cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue non-small cell lung cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

non-hodgkin lymphoma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue non-hodgkin lymphoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

non-hodgkin lymphoma cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue non-hodgkin lymphoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

non-small cell lung adenocarcinoma cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue non-small cell lung adenocarcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

non-neuronal cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

non-myelinating schwann cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue non-myelinating schwann cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

non-small cell lung cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue non-small cell lung cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Non-odorant GPCRs(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Non-odorant GPCRs(Mus musculus) pathway from the Wikipathways Pathways dataset.

Non-homologous end joining(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Non-homologous end joining(Mus musculus) pathway from the Wikipathways Pathways dataset.

Non-homologous end joining(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Non-homologous end joining(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Phase I biontransformations, non P450(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Phase I biontransformations, non P450(Mus musculus) pathway from the Wikipathways Pathways dataset.

Phase I biotransformations, non P450(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Phase I biotransformations, non P450(Homo sapiens) pathway from the Wikipathways Pathways dataset.

intracellular non-membrane-bounded organelle Gene Set

From LOCATE Predicted Protein Localization Annotations

proteins predicted to localize to the intracellular non-membrane-bounded organelle cellular component from the LOCATE Predicted Protein Localization Annotations dataset.

non-membrane-bounded organelle Gene Set

From LOCATE Predicted Protein Localization Annotations

proteins predicted to localize to the non-membrane-bounded organelle cellular component from the LOCATE Predicted Protein Localization Annotations dataset.

non-small cell lung adenocarcinoma Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease non-small cell lung adenocarcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

non-small cell lung cancer Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease non-small cell lung cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

X-linked ichthyosis with steryl-sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked ichthyosis with steryl-sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked lissencephaly 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked lissencephaly 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 58 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 58 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrogenic diabetes insipidus, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrogenic diabetes insipidus, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 45 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Creatine deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Creatine deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Properdin deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Properdin deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 63 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 63 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked severe combined immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked severe combined immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypohidrotic X-linked ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypohidrotic X-linked ectodermal dysplasia 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.

Cutis laxa, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked mental retardation 90 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked mental retardation 90 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dyskeratosis congenita X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dyskeratosis congenita X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Siderius X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nystagmus 6, congenital, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with marfanoid habitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Protoporphyria, erythropoietic, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Protoporphyria, erythropoietic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, idiopathic, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, X-linked 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, X-linked 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, X-linked 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, X-linked 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, X-linked 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, X-linked 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked infantile nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked infantile nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wilson-Turner X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wilson-Turner X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondrodysplasia punctata 2 X-linked dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chondrodysplasia punctata 2 X-linked dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hypoplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac valvular dysplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alport syndrome, X-linked recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alport syndrome, X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked lymphoproliferative syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked lymphoproliferative syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked lymphoproliferative syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked lymphoproliferative syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked recessive hypophosphatemic rickets Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked recessive hypophosphatemic rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, X-linked 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Parkinsonism with spasticity, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinsonism with spasticity, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital short bowel syndrome, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ohdo syndrome, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ohdo syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ZNF711-Related X-linked Mental Retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ZNF711-Related X-linked Mental Retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe X-linked myotubular myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial exudative vitreoretinopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined immunodeficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined immunodeficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked myopathy with postural muscle atrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hydrocephalus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tooth agenesis, selective, X-linked, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tooth agenesis, selective, X-linked, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONE DYSTROPHY 5, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONE DYSTROPHY 5, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked dominant scapuloperoneal myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked dominant scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

VACTERL association with hydrocephaly, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the VACTERL association with hydrocephaly, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked Mental Retardation 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked Mental Retardation 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 3, torsion, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 3, torsion, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor and sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked agammaglobulinemia with growth hormone deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked agammaglobulinemia with growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, X-linked, intermittent Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, X-linked, intermittent phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked periventricular heterotopia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked periventricular heterotopia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial atypical mycobacteriosis, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial atypical mycobacteriosis, type 1 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.

X-linked mental retardation 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, high-frequency sensorineural, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, high-frequency sensorineural, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked agammaglobulinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked agammaglobulinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 93 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 93 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heterotaxy, visceral, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Heterotaxy, visceral, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 96 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 96 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 98 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 98 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 99 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 99 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 72 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 72 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

X-linked hypospadias 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hypospadias 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hypospadias 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hypospadias 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondrodysplasia punctata 1, X-linked recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chondrodysplasia punctata 1, X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

lipid-linked oligosaccharides Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical lipid-linked oligosaccharides from the curated CTD Gene-Chemical Interactions dataset.

Siderius X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Siderius X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Partington X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Partington X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac valvular dysplasia, X-linked from the curated CTD Gene-Disease Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

Properdin deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Properdin deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

Opitz GBBB Syndrome, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Opitz GBBB Syndrome, X-Linked from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 34, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 34, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 30 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 30 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.

Nystagmus 1, congenital, X- linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 1, congenital, X- linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 23 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 91 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 91 from the curated CTD Gene-Disease Associations dataset.

Keratosis Follicularis Spinulosa Decalvans, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Follicularis Spinulosa Decalvans, X-Linked from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Partial Agenesis of, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Partial Agenesis of, X-Linked from the curated CTD Gene-Disease Associations dataset.

Miles-Carpenter x-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miles-Carpenter x-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 95 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 95 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 9 from the curated CTD Gene-Disease Associations dataset.

Hydrocephalus, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hydrocephalus, X-linked from the curated CTD Gene-Disease Associations dataset.

Deafness, X-Linked 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, X-Linked 5 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Endothelial, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Endothelial, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 77 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 77 from the curated CTD Gene-Disease Associations dataset.

Hypospadias 1, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypospadias 1, X-Linked from the curated CTD Gene-Disease Associations dataset.

Deafness, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Hairy Ears, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hairy Ears, Y-Linked from the curated CTD Gene-Disease Associations dataset.

Lissencephaly, X-Linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lissencephaly, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.

Tooth Agenesis, Selective, X-Linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tooth Agenesis, Selective, X-Linked, 1 from the curated CTD Gene-Disease Associations dataset.

Spondyloepiphyseal Dysplasia Tarda, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal Dysplasia Tarda, X-Linked from the curated CTD Gene-Disease Associations dataset.

Lubs X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lubs X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Hypoparathyroidism, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoparathyroidism, X-Linked from the curated CTD Gene-Disease Associations dataset.

Bulbospinal neuronopathy, X-linked recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bulbospinal neuronopathy, X-linked recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 16, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 16, X-linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Short Stature Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Short Stature from the curated CTD Gene-Disease Associations dataset.

Prostate Cancer, Hereditary, X-Linked 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, X-Linked 2 from the curated CTD Gene-Disease Associations dataset.

Creatine deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Creatine deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 20 from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 2, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 2, X-linked from the curated CTD Gene-Disease Associations dataset.

Scapuloperoneal Myopathy, X-Linked Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant from the curated CTD Gene-Disease Associations dataset.

Heterotaxy, visceral, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotaxy, visceral, X-linked from the curated CTD Gene-Disease Associations dataset.

Angioma serpiginosum, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angioma serpiginosum, X-linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 17 from the curated CTD Gene-Disease Associations dataset.

VACTERL association with hydrocephaly, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VACTERL association with hydrocephaly, X-linked from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

X-linked mental retardation Gustavson type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked mental retardation Gustavson type from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy, X-Linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy, X-Linked, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 81 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 81 from the curated CTD Gene-Disease Associations dataset.

Episodic Muscle Weakness, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic Muscle Weakness, X-Linked from the curated CTD Gene-Disease Associations dataset.

ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Sertoli cell-only syndrome, Y-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sertoli cell-only syndrome, Y-linked from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked 14 from the curated CTD Gene-Disease Associations dataset.

Mental retardation-hypotonic facies syndrome, x-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation-hypotonic facies syndrome, x-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 84 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 84 from the curated CTD Gene-Disease Associations dataset.

ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

Deafness, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, X-Linked 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, X-Linked 5 from the curated CTD Gene-Disease Associations dataset.

HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 21 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Epilepsy from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, Y-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, Y-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 78 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 78 from the curated CTD Gene-Disease Associations dataset.

X-linked sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked from the curated CTD Gene-Disease Associations dataset.

Chondrodysplasia punctata 2, X-linked dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chondrodysplasia punctata 2, X-linked dominant from the curated CTD Gene-Disease Associations dataset.

Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 73 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 73 from the curated CTD Gene-Disease Associations dataset.

Abidi X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abidi X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Panhypopituitarism X-linked Gene Set

From CTD Gene-Disease Associations

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

Lymphoproliferative Syndrome, X-Linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lymphoproliferative Syndrome, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 82 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 82 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 96 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 96 from the curated CTD Gene-Disease Associations dataset.

Genetic Diseases, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Genetic Diseases, X-Linked from the curated CTD Gene-Disease Associations dataset.

Frontotemporal Dementia, Chromosome 3-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Frontotemporal Dementia, Chromosome 3-Linked from the curated CTD Gene-Disease Associations dataset.

DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Myopathy, X-Linked, with Excessive Autophagy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, X-Linked, with Excessive Autophagy from the curated CTD Gene-Disease Associations dataset.

Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 5, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 5, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 49 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 49 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Panhypopituitarism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Panhypopituitarism from the curated CTD Gene-Disease Associations dataset.

PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, Y-Linked from the curated CTD Gene-Disease Associations dataset.

PROSTATE CANCER, HEREDITARY, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 52 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 52 from the curated CTD Gene-Disease Associations dataset.

Radial Ray Deficiency, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Radial Ray Deficiency, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 53 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 53 from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 6, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 6, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 4 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 3 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 58 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 58 from the curated CTD Gene-Disease Associations dataset.

Dystonia 3, Torsion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 3, Torsion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 63 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 63 from the curated CTD Gene-Disease Associations dataset.

Nephrolithiasis, X-Linked Recessive, with Renal Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephrolithiasis, X-Linked Recessive, with Renal Failure from the curated CTD Gene-Disease Associations dataset.

Arthrogryposis multiplex congenita, distal, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset.

MYOPATHY, CENTRONUCLEAR, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Hodgkin disease, X-linked pseudoautosomal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hodgkin disease, X-linked pseudoautosomal from the curated CTD Gene-Disease Associations dataset.

Armfield X-Linked Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Armfield X-Linked Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 42 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 42 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 93 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 93 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 94 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 94 from the curated CTD Gene-Disease Associations dataset.

X-Linked Combined Immunodeficiency Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-Linked Combined Immunodeficiency Diseases from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis congenital generalized X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis congenital generalized X-linked from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset.

GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Short Stature, Idiopathic, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset.

Agammaglobulinemia, X-linked, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Agammaglobulinemia, X-linked, type 2 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTHEMIA, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTHEMIA, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 72 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 72 from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 45 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 45 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 46 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 46 from the curated CTD Gene-Disease Associations dataset.

Spermatogenic Failure, Nonobstructive, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spermatogenic Failure, Nonobstructive, Y-Linked from the curated CTD Gene-Disease Associations dataset.

Cleft palate X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cleft palate X-linked from the curated CTD Gene-Disease Associations dataset.

CONE-ROD DYSTROPHY, X-LINKED, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONE-ROD DYSTROPHY, X-LINKED, 1 from the curated CTD Gene-Disease Associations dataset.

Prieto X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prieto X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.

EXUDATIVE VITREORETINOPATHY 2, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EXUDATIVE VITREORETINOPATHY 2, X-LINKED from the curated CTD Gene-Disease Associations dataset.

ALPORT SYNDROME, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ALPORT SYNDROME, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Hypospadias 2, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypospadias 2, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 50 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 50 from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, X-Linked from the curated CTD Gene-Disease Associations dataset.

Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, X-Linked 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.

x-linked disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

x-linked sideroblastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

x-linked hypophosphatemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked ichthyosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

x-linked hyper igm syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked hyper igm syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

x-linked nonsyndromic deafness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked myopathy with excessive autophagy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

agammaglobulinemia; genetic diseases, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease agammaglobulinemia; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, x-linked; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, x-linked; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x linked juvenile retinoschisis Gene Set

From GAD Gene-Disease Associations

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

x-linked thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

x-linked charcot-marie tooth disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked charcot-marie tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, x-linked; rett syndrome Gene Set

From GAD Gene-Disease Associations

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

brain diseases; mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; genetic diseases, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypophosphatemic rickets, x-linked dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypophosphatemic rickets, x-linked dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ichthyosis, x-linked Gene Set

From GAD Gene-Disease Associations

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

x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

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

mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked lymphoproliferative disease Gene Set

From GAD Gene-Disease Associations

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

x-linked severe combined immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, x-linked; syndrome Gene Set

From GAD Gene-Disease Associations

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

colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

x-linked adrenoleukodystrophy Gene Set

From GAD Gene-Disease Associations

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

linked Gene Set

From GeneRIF Biological Term Annotations

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

protein k33-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k33-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

histone h2a k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the histone h2a k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein k48-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein k48-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

negative regulation of protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein c-linked glycosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein c-linked glycosylation biological process from the curated GO Biological Process Annotations dataset.

dolichol-linked oligosaccharide biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the dolichol-linked oligosaccharide biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of protein k48-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein k48-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

negative regulation of protein k48-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of protein k48-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k29-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k29-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

negative regulation of histone h2a k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of histone h2a k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked mannosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked mannosylation biological process from the curated GO Biological Process Annotations dataset.

regulation of histone h2a k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of histone h2a k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein c-linked glycosylation via 2'-alpha-mannosyl-l-tryptophan Gene Set

From GO Biological Process Annotations

genes participating in the protein c-linked glycosylation via 2'-alpha-mannosyl-l-tryptophan biological process from the curated GO Biological Process Annotations dataset.

protein k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k27-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k27-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

histone h2a k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the histone h2a k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked glycosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked glycosylation biological process from the curated GO Biological Process Annotations dataset.

protein k6-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k6-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k48-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k48-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked fucosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked fucosylation biological process from the curated GO Biological Process Annotations dataset.

protein c-linked glycosylation via tryptophan Gene Set

From GO Biological Process Annotations

genes participating in the protein c-linked glycosylation via tryptophan biological process from the curated GO Biological Process Annotations dataset.

protein k11-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k11-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked glycosylation via threonine Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked glycosylation via threonine biological process from the curated GO Biological Process Annotations dataset.

protein k48-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k48-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

carnitine metabolic process, coa-linked Gene Set

From GO Biological Process Annotations

genes participating in the carnitine metabolic process, coa-linked biological process from the curated GO Biological Process Annotations dataset.

protein n-linked glycosylation via asparagine Gene Set

From GO Biological Process Annotations

genes participating in the protein n-linked glycosylation via asparagine biological process from the curated GO Biological Process Annotations dataset.

protein k27-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k27-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k11-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k11-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k29-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k29-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

regulation of protein k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k33-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k33-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

regulation of protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k6-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k6-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

enzyme linked receptor protein signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the enzyme linked receptor protein signaling pathway biological process from the curated GO Biological Process Annotations dataset.

protein n-linked glycosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein n-linked glycosylation biological process from the curated GO Biological Process Annotations dataset.

protein o-linked glycosylation via serine Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked glycosylation via serine biological process from the curated GO Biological Process Annotations dataset.

gpi-linked ephrin receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the gpi-linked ephrin receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

k63-linked polyubiquitin binding Gene Set

From GO Molecular Function Annotations

genes performing the k63-linked polyubiquitin binding molecular function from the curated GO Molecular Function Annotations dataset.

k6-linked polyubiquitin binding Gene Set

From GO Molecular Function Annotations

genes performing the k6-linked polyubiquitin binding molecular function from the curated GO Molecular Function Annotations dataset.

flavin-linked sulfhydryl oxidase activity Gene Set

From GO Molecular Function Annotations

genes performing the flavin-linked sulfhydryl oxidase activity molecular function from the curated GO Molecular Function Annotations dataset.

x-linked disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormal protein n-linked glycosylation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

x-linked dominant inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the x-linked dominant inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

x-linked recessive inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the x-linked recessive inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased urinary o-linked sialopeptides Gene Set

From HPO Gene-Disease Associations

genes associated with the increased urinary o-linked sialopeptides phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

x-linked inheritance Gene Set

From HPO Gene-Disease Associations

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

y-linked inheritance Gene Set

From HPO Gene-Disease Associations

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

Hypophosphatemic Rickets, X-Linked Dominant Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hypophosphatemic Rickets, X-Linked Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ichthyosis, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Retardation, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mental Retardation, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Genetic Diseases, Y-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Genetic Diseases, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

FAD linked oxidase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD linked oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription elongation factor A-like/Brain expressed X-linked-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription elongation factor A-like/Brain expressed X-linked-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Asparagine-linked glycosylation protein 1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Asparagine-linked glycosylation protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Heat shock transcription factor, Y-linked Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Heat shock transcription factor, Y-linked protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD/NAD-linked reductase, dimerisation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD/NAD-linked reductase, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-linked oxidase-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-linked oxidase-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Integrin-linked protein kinase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Integrin-linked protein kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-linked oxidoreductase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-linked oxidoreductase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Heat shock transcription factor, X-linked Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Heat shock transcription factor, X-linked protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-linked oxidase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-linked oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Brain-expressed X-linked protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Brain-expressed X-linked protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{autism, susceptibility to, x-linked 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism, susceptibility to, x-linked 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, x-linked 1, progressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, x-linked 1, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 84 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 84 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 81 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 81 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 82 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 82 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 89 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 89 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-parkinsonism, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-parkinsonism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?olmsted syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?olmsted syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, snyder-robinson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, snyder-robinson type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 30/47 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 30/47 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked Gene Set

From OMIM Gene-Disease Associations

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

cataract 40, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 40, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, siderius type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, siderius type phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 16, x-linked, complicated Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 16, x-linked, complicated phenotype from the curated OMIM Gene-Disease Associations dataset.

?charcot-marie-tooth disease, x-linked dominant, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?charcot-marie-tooth disease, x-linked dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, x-linked recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, x-linked recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency, x-linked, with hyper-igm Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, x-linked, with hyper-igm phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, fraxe type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, fraxe type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoparathyroidism, x-linked Gene Set

From OMIM Gene-Disease Associations

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

{autism susceptibility, x-linked 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{graves disease, susceptibility to, x-linked} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {graves disease, susceptibility to, x-linked} phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, y-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, y-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, intermittent Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, intermittent phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy, x-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

lissencephaly, x-linked Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked, with isolated growth hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with isolated growth hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 91 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 91 phenotype from the curated OMIM Gene-Disease Associations dataset.

lissencephaly, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

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

epilepsy, x-linked, with variable learning disabilities and behavior disorders Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, x-linked, with variable learning disabilities and behavior disorders phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 90 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 90 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 98 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 98 phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation-hypotonic facies syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-hypotonic facies syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

spermatogenic failure, y-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spermatogenic failure, y-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spermatogenic failure, y-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spermatogenic failure, y-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

exudative vitreoretinopathy 2, x-linked Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

hypospadias 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypospadias 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility, x-linked 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 78 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 78 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 72 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 72 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

chondrodysplasia punctata, x-linked dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the chondrodysplasia punctata, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 52 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 52 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 53 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 53 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 50 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 50 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 58 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 58 phenotype from the curated OMIM Gene-Disease Associations dataset.

properdin deficiency, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the properdin deficiency, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 21/34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 21/34 phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, x-linked 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, x-linked 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 1, hypohidrotic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 1, hypohidrotic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 2, x-linked Gene Set

From OMIM Gene-Disease Associations

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

keratosis follicularis spinulosa decalvans, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratosis follicularis spinulosa decalvans, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia with beta-thalassemia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia with beta-thalassemia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?stocco dos santos x-linked mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?stocco dos santos x-linked mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

ohdo syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ohdo syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 77 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 77 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, congenital, with fiber-type disproportion, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, congenital, with fiber-type disproportion, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{asperger syndrome susceptibility, x-linked 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asperger syndrome susceptibility, x-linked 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

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

spinocerebellar ataxia, x-linked 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, x-linked 5 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.

mental retardation, x-linked, with short stature Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with short stature phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 92 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 92 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 93 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 93 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 96 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 96 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 97 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 97 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 94 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 94 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 95 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 95 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 99 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 99 phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypospadias 4, x-linked, susceptibilty to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypospadias 4, x-linked, susceptibilty to} phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 34, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 34, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy, progressive x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, endothelial, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, sideroblastic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, sideroblastic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

vacterl association, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the vacterl association, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

combined immunodeficiency, x-linked, moderate Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined immunodeficiency, x-linked, moderate phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus, infantile periodic alternating, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus, infantile periodic alternating, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal myopathy, x-linked dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal myopathy, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 2, x-linked Gene Set

From OMIM Gene-Disease Associations

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

agammaglobulinemia, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the agammaglobulinemia, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

agammaglobulinemia, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

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

chondrodysplasia punctata, x-linked recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the chondrodysplasia punctata, x-linked recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 1, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 1, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphoproliferative syndrome, x-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphoproliferative syndrome, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphoproliferative syndrome, x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

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

episodic muscle weakness, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic muscle weakness, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked dominant, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocythemia, x-linked Gene Set

From OMIM Gene-Disease Associations

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

immunodeficiency 34, mycobacteriosis, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 34, mycobacteriosis, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, x-linked 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

myotubular myopathy, x-linked Gene Set

From OMIM Gene-Disease Associations

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

protoporphyria, erythropoietic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the protoporphyria, erythropoietic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 6, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

spermatogenic failure, x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

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

macular degeneration, x-linked atrophic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular degeneration, x-linked atrophic phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility, x-linked 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystropy, x-linked, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystropy, x-linked, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

subcortical laminal heteropia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the subcortical laminal heteropia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (incomplete), 2a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (incomplete), 2a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, y-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, y-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility, x-linked 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypophosphatemic rickets, x-linked dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypophosphatemic rickets, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral-cerebellar-coloboma syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral-cerebellar-coloboma syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 63 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 63 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac valvular dysplasia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac valvular dysplasia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 101 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 101 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 100 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 100 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 49 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 49 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 6, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 6, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, x-linked 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, x-linked 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, x-linked 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

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

deafness, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

panhypopituitarism, x-linked Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 29 and others Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 29 and others phenotype from the curated OMIM Gene-Disease Associations dataset.

?parkinsonism with spasticity, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?parkinsonism with spasticity, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa, x-linked recessive, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa, x-linked recessive, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskeratosis congenita, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskeratosis congenita, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{mycobacerium tuberculosis, susceptibility, x-linked} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {mycobacerium tuberculosis, susceptibility, x-linked} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypospadias 2, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypospadias 2, x-linked 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.

ichthyosis, x-linked Gene Set

From OMIM Gene-Disease Associations

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

severe combined immunodeficiency, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?hairy ears, y-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hairy ears, y-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 5, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 5, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{asperger syndrome susceptibility, x-linked 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asperger syndrome susceptibility, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{diabetes mellitus, insulin-dependent, x-linked} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {diabetes mellitus, insulin-dependent, x-linked} phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodysregulation, polyendocrinopathy, and enteropathy, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodysregulation, polyendocrinopathy, and enteropathy, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

Coenzyme A linked carnitine metabolism Gene Set

From PANTHER Pathways

proteins participating in the Coenzyme A linked carnitine metabolism pathway from the PANTHER Pathways dataset.

Integrin-linked kinase signaling Gene Set

From PID Pathways

proteins participating in the Integrin-linked kinase signaling pathway from the PID Pathways dataset.

Asparagine N-linked glycosylation Gene Set

From Reactome Pathways

proteins participating in the Asparagine N-linked glycosylation pathway from the Reactome Pathways dataset.

O-linked glycosylation Gene Set

From Reactome Pathways

proteins participating in the O-linked glycosylation pathway from the Reactome Pathways dataset.

O-linked glycosylation of mucins Gene Set

From Reactome Pathways

proteins participating in the O-linked glycosylation of mucins pathway from the Reactome Pathways dataset.

Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set

From Reactome Pathways

proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways dataset.

Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Set

From Reactome Pathways

proteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways dataset.

X-linked hypophosphatemia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease X-linked hypophosphatemia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

X-linked agammaglobulinaemia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease X-linked agammaglobulinaemia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.