ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis

Clear Filter

Results for "ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis": 1002 gene sets

Name
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis phenotype from the curated OMIM Gene-Disease Associations dataset.
Neonatal ichthyosis-sclerosing cholangitis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal ichthyosis-sclerosing cholangitis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sclerosing cholangitis and ulcerative colitis (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sclerosing cholangitis and ulcerative colitis (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sclerosing cholangitis and ulcerative colitis (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sclerosing cholangitis and ulcerative colitis (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.
keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set From OMIM Gene-Disease Associations genes associated with the keratosis linearis with ichthyosis congenita and sclerosing keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.
Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cholangitis, Sclerosing Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholangitis, Sclerosing from the curated CTD Gene-Disease Associations dataset.
Cholangitis, Sclerosing Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Cholangitis, Sclerosing in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
sclerosing cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene Set From GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cirrhosis, biliary primary; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ulcerative colitis; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease ulcerative colitis; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
primary sclerosing cholangitis Gene Set From GAD Gene-Disease Associations genes associated with the disease primary sclerosing cholangitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sclerosing cholangitis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sclerosing cholangitis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Cholangitis, Sclerosing Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cholangitis, Sclerosing phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
cholangitis, primary sclerosing Gene Set From OMIM Gene-Disease Associations genes associated with the cholangitis, primary sclerosing phenotype from the curated OMIM Gene-Disease Associations dataset.
Cholangitis, Sclerosing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cholangitis, Sclerosing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Sclerosing Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Sclerosing Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Cholangitis, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Cholangitis, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Igg4-Related Sclerosing Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Igg4-Related Sclerosing Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Sclerosing Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Sclerosing Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing cholangitis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sclerosing cholangitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary sclerosing cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary sclerosing cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated neonatal sclerosing cholangitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated neonatal sclerosing cholangitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Autoimmune hepatitis in primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autoimmune hepatitis in primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Liver transplant-free survival in primary sclerosing cholangitis (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver transplant-free survival in primary sclerosing cholangitis (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cholangiocarcinoma in primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cholangiocarcinoma in primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cholangiocarcinoma in primary sclerosing cholangitis (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cholangiocarcinoma in primary sclerosing cholangitis (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Colorectal carcinoma in primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colorectal carcinoma in primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis follicularis-alopecia-photophobia syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ichthyosis follicularis-alopecia-photophobia syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set From OMIM Gene-Disease Associations genes associated with the exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated OMIM Gene-Disease Associations dataset.
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa Of Siemens-Like Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa Of Siemens-Like in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
vacuoles Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term vacuoles in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
autophagic vacuoles Gene Set From HPO Gene-Disease Associations genes associated with the autophagic vacuoles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rimmed vacuoles Gene Set From HPO Gene-Disease Associations genes associated with the rimmed vacuoles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
brain vacuoles Gene Set From MPO Gene-Phenotype Associations gene mutations causing the brain vacuoles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular dystrophy with rimmed vacuoles Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.
Rimmed Vacuoles On Biopsy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rimmed Vacuoles On Biopsy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
brain vacuoles Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the brain vacuoles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Distal myopathy with rimmed vacuoles Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rimmed vacuoles Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rimmed vacuoles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset.
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.
alopecia and lumbar herniated disk Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia and lumbar herniated disk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set From OMIM Gene-Disease Associations genes associated with the macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated OMIM Gene-Disease Associations dataset.
t-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the t-cell immunodeficiency, congenital alopecia, and nail dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease T-cell immunodeficiency, congenital alopecia, and nail dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alopecia, neurologic defects, and endocrinopathy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease T-cell immunodeficiency, congenital alopecia, and nail dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Palmoplantar keratoderma and congenital alopecia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Palmoplantar keratoderma and congenital alopecia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Palmoplantar keratoderma and congenital alopecia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Palmoplantar keratoderma and congenital alopecia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, spastic quadriplegia, and mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratitis ichthyosis and deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Keratitis ichthyosis and deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cholangitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholangitis from the curated CTD Gene-Disease Associations dataset.
cholangitis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cholangitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
acute cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
suppurative cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease suppurative cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ascending cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ascending cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cholangitis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cholangitis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cholangitis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cholangitis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Biliary Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Biliary Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Suppurative Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Suppurative Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bacterial Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bacterial Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Granulomatous Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Granulomatous Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Obstructive Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Obstructive Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cholangitis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cholangitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary biliary cholangitis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Primary biliary cholangitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary biliary cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Suppurative cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Suppurative cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ascending cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ascending cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acute cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary biliary cholangitis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary biliary cholangitis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary biliary cholangitis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary biliary cholangitis 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary biliary cholangitis 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cryptosporidiosis-chronic cholangitis-liver disease syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cryptosporidiosis-chronic cholangitis-liver disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary biliary cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary biliary cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy from the curated CTD Gene-Disease Associations dataset.
sost-related sclerosing bone dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sclerosing liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pulmonary sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute sclerosing panencephalitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute sclerosing panencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sost-related sclerosing bone dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sclerosing keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sclerosing hepatic carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing hepatic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease dawson's inclusion body encephalitis; subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panencephalitis, subacute sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease panencephalitis, subacute sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sclerosing Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term sclerosing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Subacute Sclerosing Panencephalitis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Subacute Sclerosing Panencephalitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Subacute Sclerosing Panencephalitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Sclerosing Panencephalitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Sclerosing Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Sclerosing Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Igg4-Related Sclerosing Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Igg4-Related Sclerosing Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Polycystic Adenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Polycystic Adenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Peritonitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Epithelioid Fibrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Epithelioid Fibrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breast Sclerosing Adenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breast Sclerosing Adenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spindle Cell/Sclerosing Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spindle Cell/Sclerosing Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Lymphocytic Lobulitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Lymphocytic Lobulitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Sclerosing Bone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Sclerosing Bone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Sclerosing Sialadenitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Sclerosing Sialadenitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Encapsulating Peritonitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Encapsulating Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Stromal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovarian Sclerosing Stromal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Sclerosing Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
SOST-related sclerosing bone dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease SOST-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Subacute sclerosing panencephalitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute sclerosing panencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
SOST-related sclerosing bone dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease SOST-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulmonary sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing hepatic carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing hepatic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nonencapsulated sclerosing carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nonencapsulated sclerosing carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary sclerosing poikiloderma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sclerosing poikiloderma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alopecia universalis congenita Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia universalis congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia-Mental Retardation Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
Alopecia-Mental Retardation Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Alopecia, Androgenetic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia, Androgenetic, 2 from the curated CTD Gene-Disease Associations dataset.
Alopecia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia from the curated CTD Gene-Disease Associations dataset.
Alopecia universalis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia universalis from the curated CTD Gene-Disease Associations dataset.
Alopecia, Androgenetic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia, Androgenetic, 3 from the curated CTD Gene-Disease Associations dataset.
Alopecia Areata Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia Areata from the curated CTD Gene-Disease Associations dataset.
Alopecia Areata Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Alopecia Areata in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
alopecia areata Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease alopecia areata in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
alopecia Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease alopecia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
alopecia universalis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease alopecia universalis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
alopecia areata Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alopecia areata in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alopecia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alopecia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alopecia universalis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alopecia universalis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alopecia areata; Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia areata; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alopecia areata; autoimmune diseases; polyendocrinopathies, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia areata; autoimmune diseases; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alopecia; Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alopecia Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
supernumerary teeth, alopecia Gene Set From GAD Gene-Disease Associations genes associated with the disease supernumerary teeth, alopecia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alopecia areata Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia areata in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alopecia areata; autoimmune diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia areata; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alopecia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term alopecia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Alopecia areata Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Alopecia areata phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Adverse response to chemotherapy in breast cancer (alopecia) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+epirubicin+/-5FU) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+epirubicin+/-5FU) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+doxorubicin+/-5FU) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+doxorubicin+/-5FU) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (paclitaxel) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (paclitaxel) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (anti-microtubule) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (anti-microtubule) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
alopecia areata Gene Set From GWASdb SNP-Disease Associations genes associated with the disease alopecia areata in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
alopecia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease alopecia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
alopecia areata Gene Set From GWASdb SNP-Phenotype Associations genes associated with the alopecia areata phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
alopecia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the alopecia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
alopecia of scalp Gene Set From HPO Gene-Disease Associations genes associated with the alopecia of scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophic, patchy alopecia Gene Set From HPO Gene-Disease Associations genes associated with the atrophic, patchy alopecia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
alopecia Gene Set From HPO Gene-Disease Associations genes associated with the alopecia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
alopecia universalis Gene Set From HPO Gene-Disease Associations genes associated with the alopecia universalis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
patchy alopecia Gene Set From HPO Gene-Disease Associations genes associated with the patchy alopecia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
alopecia totalis Gene Set From HPO Gene-Disease Associations genes associated with the alopecia totalis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive alopecia Gene Set From HPO Gene-Disease Associations genes associated with the progressive alopecia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
alopecia areata Gene Set From HPO Gene-Disease Associations genes associated with the alopecia areata phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
scarring alopecia of scalp Gene Set From HPO Gene-Disease Associations genes associated with the scarring alopecia of scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Alopecia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alopecia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alopecia Areata Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alopecia Areata phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
alopecia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the alopecia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
alopecia universalis Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia universalis phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia-mental retardation syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia-mental retardation syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia-mental retardation syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia-mental retardation syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia-mental retardation syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia-mental retardation syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia areata 2 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia areata 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia areata 1 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia areata 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia, androgenetic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia, androgenetic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia, androgenetic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia, androgenetic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
alopecia, androgenetic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the alopecia, androgenetic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Androgenetic Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Androgenetic Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scarring Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scarring Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Fibrosing Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Fibrosing Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Postmenopausal Frontal Fibrosing Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Postmenopausal Frontal Fibrosing Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alopecia Congenita Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alopecia Congenita in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mandibulofacial Dysostosis With Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mandibulofacial Dysostosis With Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophic, Patchy Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophic, Patchy Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alopecia Areata 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alopecia Areata 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Centrifugal Cicatricial Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Centrifugal Cicatricial Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Scarring Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Scarring Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Female Pattern Alopecia (Disorder) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Pattern Alopecia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Other Alopecia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Scarring Alopecia Of Scalp Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scarring Alopecia Of Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Patchy Alopecia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patchy Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Alopecia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
alopecia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the alopecia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Alopecia areata Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alopecia areata from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Alopecia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alopecia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Androgenic alopecia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Androgenic alopecia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Androgenic alopecia Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Androgenic alopecia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Alopecia Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Alopecia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Alopecia areata Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Alopecia areata in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Alopecia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alopecia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alopecia areata Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alopecia areata in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Androgenic alopecia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Androgenic alopecia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
alopecia-mental retardation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alopecia-mental retardation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alopecia universalis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alopecia universalis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mandibulofacial dysostosis with alopecia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mandibulofacial dysostosis with alopecia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
alopecia-mental retardation syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alopecia-mental retardation syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diffuse alopecia areata Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse alopecia areata in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alopecia universalis congenita Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alopecia universalis congenita phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alopecia-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alopecia-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alopecia areata Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alopecia areata phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Persistent chemotherapy-induced alopecia in breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Persistent chemotherapy-induced alopecia in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Frontal fibrosing alopecia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Frontal fibrosing alopecia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adverse response to chemotherapy in breast cancer (alopecia) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+epirubicin+/-5FU) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+epirubicin+/-5FU) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+doxorubicin+/-5FU) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+doxorubicin+/-5FU) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (paclitaxel) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (paclitaxel) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (docetaxel) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (docetaxel) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adverse response to chemotherapy in breast cancer (alopecia) (anti-microtubule) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to chemotherapy in breast cancer (alopecia) (anti-microtubule) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alopecia areata Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alopecia areata phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thiopurine-induced alopecia in inflammatory bowel disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thiopurine-induced alopecia in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thiopurine-induced severe alopecia in inflammatory bowel disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thiopurine-induced severe alopecia in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 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.
Triglyceride storage disease with ichthyosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lamellar ichthyosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lamellar ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis prematurity syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis prematurity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis with hypotrichosis, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis with hypotrichosis, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Harlequin type ichthyosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Harlequin type ichthyosis from the curated CTD Gene-Disease Associations dataset.
Lamellar ichthyosis, type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lamellar ichthyosis, type 2 from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Lamellar, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Lamellar, 5 from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis from the curated CTD Gene-Disease Associations dataset.
Ichthyosis Bullosa of Siemens Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis Bullosa of Siemens from the curated CTD Gene-Disease Associations dataset.
Ichthyosis Vulgaris Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis Vulgaris from the curated CTD Gene-Disease Associations dataset.
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 from the curated CTD Gene-Disease Associations dataset.
Ichthyosis follicularis atrichia photophobia syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis follicularis atrichia photophobia syndrome from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Lamellar Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Lamellar from the curated CTD Gene-Disease Associations dataset.
Ichthyosis hystrix, Curth Macklin type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis hystrix, Curth Macklin type from the curated CTD Gene-Disease Associations dataset.
Ichthyosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis from the curated CTD Gene-Disease Associations dataset.
Ichthyosis prematurity syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis prematurity syndrome 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.
Lamellar ichthyosis, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lamellar ichthyosis, type 3 from the curated CTD Gene-Disease Associations dataset.
x-linked ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association 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.
ichthyosis vulgaris Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ichthyosis vulgaris in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ichthyosis Gene Set From GAD Gene-Disease Associations genes associated with the disease ichthyosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ichthyosis vulgaris Gene Set From GAD Gene-Disease Associations genes associated with the disease ichthyosis vulgaris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, atopic; ichthyosis vulgaris Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, atopic; ichthyosis vulgaris 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.
lamellar ichthyosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lamellar ichthyosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, allergic contact; hypersensitivity; hypersensitivity, immediate; ichthyosis vulgaris Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, allergic contact; hypersensitivity; hypersensitivity, immediate; ichthyosis vulgaris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ichthyosis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term ichthyosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
ichthyosis Gene Set From HPO Gene-Disease Associations genes associated with the ichthyosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.
Ichthyosis Vulgaris Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ichthyosis Vulgaris phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ichthyosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ichthyosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
ichthyosis, cyclic, with epidermolytic hyperkeratosis Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, cyclic, with epidermolytic hyperkeratosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hystrix-like ichthyosis with deafness Gene Set From OMIM Gene-Disease Associations genes associated with the hystrix-like ichthyosis with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis vulgaris Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis vulgaris phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis prematurity syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis prematurity syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis histrix, curth-macklin type Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis histrix, curth-macklin type phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 4a Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 4a phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, autosomal recessive 4b (harlequin) Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, autosomal recessive 4b (harlequin) phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis with confetti Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis with confetti phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 7 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 8 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 9 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 10 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, congenital, autosomal recessive 11 Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, congenital, autosomal recessive 11 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.
ichthyosis bullosa of siemens Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis bullosa of siemens phenotype from the curated OMIM Gene-Disease Associations dataset.
keratitis-ichthyosis-deafness syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the keratitis-ichthyosis-deafness syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
vohwinkel syndrome with ichthyosis Gene Set From OMIM Gene-Disease Associations genes associated with the vohwinkel syndrome with ichthyosis phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) pathway from the Reactome Pathways dataset.
Triglyceride Storage Disease With Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triglyceride Storage Disease With Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Harlequin Type Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Harlequin Type Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Congenita Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Congenita in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lamellar Ichthyosis, Type 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lamellar Ichthyosis, Type 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Bullosa Of Siemens Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Bullosa Of Siemens in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratitis-Ichthyosis-Deafness Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratitis-Ichthyosis-Deafness Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Vulgaris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Vulgaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bathing Suit Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bathing Suit Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Ichthyosis Vulgaris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Ichthyosis Vulgaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Follicularis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Follicularis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Congenital Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Hystrix Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ichthyosis Hystrix in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratinopathic Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratinopathic Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Follicular Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Follicular Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Syndromic Recessive X-Linked Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Syndromic Recessive X-Linked Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ichthyosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Ichthyosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS) pathway from the Reactome Pathways 2024 dataset.
Ichthyosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ichthyosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive congenital ichthyosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive congenital ichthyosis 4B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ichthyosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked ichthyosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ichthyosis vulgaris Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ichthyosis vulgaris in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 4B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 4A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 4A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive congenital ichthyosis 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant keratitis-ichthyosis-deafness syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant keratitis-ichthyosis-deafness syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive congenital ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive congenital ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lamellar ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lamellar ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Keratoderma-ichthyosis-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Keratoderma-ichthyosis-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital ichthyosis of skin Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital ichthyosis of skin phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis linearis circumflexa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis linearis circumflexa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis prematurity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis prematurity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis bullosa of Siemens Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis bullosa of Siemens phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Exfoliative ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Exfoliative ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Annular epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Annular epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ichthyosis vulgaris Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ichthyosis vulgaris phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant keratitis-ichthyosis-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant ichthyosis vulgaris Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant ichthyosis vulgaris phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive keratitis-ichthyosis-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive keratitis-ichthyosis-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LEUKOCYTE ADHESION DEFICIENCY, TYPE III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LEUKOCYTE ADHESION DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukocyte adhesion deficiency type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukocyte adhesion deficiency type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukocyte adhesion deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukocyte adhesion deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukocyte Adhesion Deficiency, Type III Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte Adhesion Deficiency, Type III from the curated CTD Gene-Disease Associations dataset.
Leukocyte Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte Disorders from the curated CTD Gene-Disease Associations dataset.
Leukocyte adhesion deficiency type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte adhesion deficiency type 1 from the curated CTD Gene-Disease Associations dataset.
Leukocyte-Adhesion Deficiency Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte-Adhesion Deficiency Syndrome from the curated CTD Gene-Disease Associations dataset.
Leukocyte Count Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Leukocyte Count in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
leukocyte disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease leukocyte disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
leukocyte disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease leukocyte disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
leukocyte-adhesion deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leukocyte-adhesion deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
leukocyte adhesion deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leukocyte adhesion deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
leukocyte disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leukocyte disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
leukocyte adhesion deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease leukocyte adhesion deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukocyte count Gene Set From GAD Gene-Disease Associations genes associated with the disease leukocyte count in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukocyte Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term leukocyte in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte chemotaxis involved in inflammatory response Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte chemotaxis involved in inflammatory response biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte migration Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte migration biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte migration involved in inflammatory response Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte migration involved in inflammatory response biological process from the curated GO Biological Process Annotations 2015 dataset.
myeloid leukocyte cytokine production Gene Set From GO Biological Process Annotations 2015 genes participating in the myeloid leukocyte cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2015 dataset.
myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte activation Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte activation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte degranulation Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte degranulation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte adhesive activation Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte adhesive activation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of myeloid leukocyte cytokine production involved in immune response Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of myeloid leukocyte cytokine production involved in immune response biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte aggregation Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte aggregation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
myeloid leukocyte migration Gene Set From GO Biological Process Annotations 2015 genes participating in the myeloid leukocyte migration biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte homeostasis Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
myeloid leukocyte activation Gene Set From GO Biological Process Annotations 2015 genes participating in the myeloid leukocyte activation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte migration involved in immune response Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte migration involved in immune response biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte activation involved in immune response Gene Set From GO Biological Process Annotations 2015 genes participating in the leukocyte activation involved in immune response biological process from the curated GO Biological Process Annotations 2015 dataset.
leukocyte disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease leukocyte disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormal leukocyte count Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal leukocyte count Gene Set From HPO Gene-Disease Associations genes associated with the abnormal leukocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
elevated leukocyte alkaline phosphatase Gene Set From HPO Gene-Disease Associations genes associated with the elevated leukocyte alkaline phosphatase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Leukocyte Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Leukocyte Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Leukocyte tyrosine kinase receptor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Leukocyte tyrosine kinase receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Leukocyte surface antigen CD47 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Leukocyte surface antigen CD47 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Leukocyte cell-derived chemotaxin 2, chordata Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Leukocyte cell-derived chemotaxin 2, chordata protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Leukocyte cell-derived chemotaxin 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Leukocyte cell-derived chemotaxin 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Leukocyte elastase inhibitor (serpin B1) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Leukocyte elastase inhibitor (serpin B1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Leukocyte-specific transcript 1, LST-1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Leukocyte-specific transcript 1, LST-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Alpha-1B-glycoprotein/leukocyte immunoglobulin-like receptor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha-1B-glycoprotein/leukocyte immunoglobulin-like receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
leukocyte transendothelial migration Gene Set From KEGG Pathways proteins participating in the leukocyte transendothelial migration pathway from the KEGG Pathways dataset.
abnormal myeloid leukocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal myeloid leukocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased leukocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased leukocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal leukocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal leukocyte adhesion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte adhesion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased leukocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased leukocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal leukocyte tethering or rolling Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte tethering or rolling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal leukocyte migration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal leukocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal leukocyte physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
leukocyte adhesion deficiency, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the leukocyte adhesion deficiency, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
[telomere length, mean leukocyte] Gene Set From OMIM Gene-Disease Associations genes associated with the [telomere length, mean leukocyte] phenotype from the curated OMIM Gene-Disease Associations dataset.
leukocyte adhesion deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leukocyte adhesion deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leukocyte Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term leukocyte in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
leukocyte Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue leukocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
leukocyte Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue leukocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
polymorphonuclear leukocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue polymorphonuclear leukocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
leukocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue leukocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Leukocyte Adhesion Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leukocyte Adhesion Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Leukocyte Adherence Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Leukocyte Adherence Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Telomere Length, Mean Leukocyte Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Telomere Length, Mean Leukocyte in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reduced Leukocyte Alkaline Phosphatase Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Leukocyte Alkaline Phosphatase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Leukocyte Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Leukocyte Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
negative regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte chemotaxis involved in inflammatory response Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte chemotaxis involved in inflammatory response biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2023 dataset.
myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte aggregation Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte aggregation biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of myeloid leukocyte cytokine production involved in immune response Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of myeloid leukocyte cytokine production involved in immune response biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2023 genes participating in the myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
decreased leukocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased leukocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased leukocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased leukocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal leukocyte adhesion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte adhesion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enhanced leukocyte tethering or rolling Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced leukocyte tethering or rolling phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal leukocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal leukocyte morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired leukocyte tethering or rolling Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired leukocyte tethering or rolling phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal leukocyte physiology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal leukocyte migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal myeloid leukocyte morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal myeloid leukocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal leukocyte tethering or rolling Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte tethering or rolling phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired leukocyte migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired leukocyte migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enhanced leukocyte migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced leukocyte migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased leukocyte cell number Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased leukocyte cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
decreased leukocyte cell number Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased leukocyte cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Leukocyte intrinsic Hippo pathway functions Gene Set From WikiPathways Pathways 2024 proteins participating in the Leukocyte intrinsic Hippo pathway functions pathway from the WikiPathways Pathways 2024 dataset.
negative regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte chemotaxis involved in inflammatory response Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte chemotaxis involved in inflammatory response biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte migration Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte migration biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2025 dataset.
myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte cell-cell adhesion Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte tethering or rolling Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte tethering or rolling biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte aggregation Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte aggregation biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte adhesion to arterial endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte mediated cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte activation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte activation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of myeloid leukocyte cytokine production involved in immune response Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of myeloid leukocyte cytokine production involved in immune response biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte chemotaxis Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte adhesion to vascular endothelial cell Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of myeloid leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of myeloid leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2025 genes participating in the myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2025 genes participating in the leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of myeloid leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of myeloid leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte degranulation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte degranulation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of leukocyte apoptotic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of leukocyte apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of leukocyte mediated immunity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of leukocyte mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
Leukocyte disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Leukocyte disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Leukocyte disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Leukocyte disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukocyte disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukocyte disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukocyte adhesion deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukocyte adhesion deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukocyte adhesion deficiency 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukocyte adhesion deficiency 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukocyte adhesion deficiency 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukocyte adhesion deficiency 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukocyte adhesion deficiency 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukocyte adhesion deficiency 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukocyte Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Leukocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Leukocyte Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Leukocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Leukocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Leukocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Polymorphonuclear leukocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Polymorphonuclear leukocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Leukocyte adhesion deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leukocyte adhesion deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lazy leukocyte syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lazy leukocyte syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leukocyte telomere length Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Leukocyte telomere length phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Leukocyte transendothelial migration Gene Set From KEGG Pathways 2026 proteins participating in the Leukocyte transendothelial migration pathway from the KEGG Pathways 2026 dataset.
LEUKOCYTE INTERLEUKIN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the LEUKOCYTE INTERLEUKIN drug from theDGIdb Drug Targets 2026 dataset.
MULTI-SUBTYPE NATURAL HUMAN LEUKOCYTE INTERFERON ALPHA Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MULTI-SUBTYPE NATURAL HUMAN LEUKOCYTE INTERFERON ALPHA drug from theDGIdb Drug Targets 2026 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Basic cell groups and regions Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
head and face region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
telomeres telomerase cellular aging and immortality Gene Set From Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.
mcalpain and friends in cell motility Gene Set From Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.
role of ppar-gamma coactivators in obesity and thermogenesis Gene Set From Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hypoxia and p53 in the cardiovascular system Gene Set From Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
role of erbb2 in signal transduction and oncology Gene Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.
nfat and hypertrophy of the heart Gene Set From Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.
acetylation and deacetylation of rela in nucleus Gene Set From Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.
thrombin signaling and protease-activated receptors Gene Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
role of ß-arrestins in the activation and targeting of map kinases Gene Set From Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set From Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.
btg family proteins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set From Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.
endocytotic role of ndk phosphins and dynamin Gene Set From Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.
regulation of eif-4e and p70s6 kinase Gene Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.
yaci and bcma stimulation of b cell immune responses Gene Set From Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.
lck and fyn tyrosine kinases in initiation of tcr activation Gene Set From Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.
hiv-1 nef: negative effector of fas and tnf Gene Set From Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set From Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.
ucalpain and friends in cell spread Gene Set From Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.
ionomycin and phorbal ester signaling pathway Gene Set From Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.
carm1 and regulation of the estrogen receptor Gene Set From Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.
phosphoinositides and their downstream targets Gene Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
akap95 role in mitosis and chromosome dynamics Gene Set From Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.
transcription factor creb and its extracellular signals Gene Set From Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
the igf-1 receptor and longevity Gene Set From Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.
cdc25 and chk1 regulatory pathway in response to dna damage Gene Set From Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.
human cytomegalovirus and map kinase pathways Gene Set From Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.
influence of ras and rho proteins on g1 to s transition Gene Set From Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.
proteolysis and signaling pathway of notch Gene Set From Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.
apoptotic dna-fragmentation and tissue homeostasis Gene Set From Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.
ion channels and their functional role in vascular endothelium Gene Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.
links between pyk2 and map kinases Gene Set From Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.
opposing roles of aif in apoptosis and cell survival Gene Set From Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.
degradation of the rar and rxr by the proteasome Gene Set From Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set From Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.
role of brca1 brca2 and atr in cancer susceptibility Gene Set From Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.
chrebp regulation by carbohydrates and camp Gene Set From Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.
pten dependent cell cycle arrest and apoptosis Gene Set From Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
CIITA-18437201-Raji B cells and iDC-human Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
VDR-23401126-LCL-AND-THP1-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vater association with macrocephaly and ventriculomegaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microtia, hearing impairment, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined cellular and humoral immune defects with granulomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss 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.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multicentric osteolysis, nodulosis and arthropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stapes ankylosis with broad thumb and toes Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, short stature, and impaired glucose metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy dilated with woolly hair and keratoderma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal 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.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone fragility with contractures, arterial rupture, and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor v and factor viii, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary Paragangliomas and Pheochromocytomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas 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.
Band-like calcification with simplified gyration and polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 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.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, juvenile, with microcornea and glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, deafness, and narcolepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary leiomyomatosis and renal cell cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Monocyte and dendritic cell deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, hiatal hernia and nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined malonic and methylmalonic aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis Gyrata syndrome of Beare and Stevenson Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation 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.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniosynostosis and dental anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Obesity, hyperphagia, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebroretinal microangiopathy with calcifications and cysts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alacrima, achalasia, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, normal intelligence and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Calcification of joints and arteries Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis and recurrent skin vesicles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pineal hyperplasia AND diabetes mellitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Morbid obesity and spermatogenic failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sensory and autonomic neuropathy type IIA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of factor V and factor VIII, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Camptodactyly, tall stature, and hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth deficiency and mental retardation with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype 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.
Combined deficiency of sialidase AND beta galactosidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase 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.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix part Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set From CORUM Protein Complexes proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set From CORUM Protein Complexes proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.
6S methyltransferase and RG-containing Sm proteins complex Gene Set From CORUM Protein Complexes proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.
Remodeling and spacing factor (RSF) complex Gene Set From CORUM Protein Complexes proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.
PBAF complex (Polybromo- and BAF containing complex) Gene Set From CORUM Protein Complexes proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.
Cleavage and polyadenylation factor (CPSF) Gene Set From CORUM Protein Complexes proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Nucleic and chromatin Fanconi complex Gene Set From CORUM Protein Complexes proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set From CORUM Protein Complexes proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.
20S methylosome and RG-containing Sm protein complex Gene Set From CORUM Protein Complexes proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.
Amino Acids, Peptides, and Proteins Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.
Bile Acids and Salts Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.
Prime and Bond NT Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.
drospirenone and ethinyl estradiol combination Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.
Hypophosphatemic Rickets And Hyperparathyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
Synovitis granulomatous with uveitis and cranial neuropathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.
Hereditary Sensory and Motor Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.
Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.
Combined Cellular And Humoral Immune Defects With Granulomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set

ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis Gene Set

Neonatal ichthyosis-sclerosing cholangitis syndrome Gene Set

Sclerosing cholangitis and ulcerative colitis (combined) Gene Set

Sclerosing cholangitis and ulcerative colitis (combined) Gene Set

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set

Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma Gene Set

Cholangitis, Sclerosing Gene Set

Cholangitis, Sclerosing Gene Set

sclerosing cholangitis Gene Set

biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene Set

cirrhosis, biliary primary; cholangitis, sclerosing Gene Set

cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative Gene Set

arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set

ulcerative colitis; cholangitis, sclerosing Gene Set

bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing Gene Set

lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit Gene Set

autoimmune diseases; cholangitis, sclerosing Gene Set

cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis Gene Set

cholangitis, sclerosing; disease progression Gene Set

cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary Gene Set

cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set

primary sclerosing cholangitis Gene Set

cholangitis, sclerosing; Gene Set

bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; Gene Set

cholangitis, sclerosing Gene Set

Primary sclerosing cholangitis Gene Set

sclerosing cholangitis Gene Set

Cholangitis, Sclerosing Gene Set

cholangitis, primary sclerosing Gene Set

Cholangitis, Sclerosing Gene Set

Primary Sclerosing Cholangitis Gene Set

Sclerosing Cholangitis, Neonatal Gene Set

Igg4-Related Sclerosing Cholangitis Gene Set

Secondary Sclerosing Cholangitis Gene Set

Sclerosing cholangitis Gene Set

Sclerosing cholangitis Gene Set

Primary sclerosing cholangitis Gene Set

Isolated neonatal sclerosing cholangitis Gene Set

Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) Gene Set

Primary sclerosing cholangitis Gene Set

Autoimmune hepatitis in primary sclerosing cholangitis Gene Set

Liver transplant-free survival in primary sclerosing cholangitis (time to event) Gene Set

Cholangiocarcinoma in primary sclerosing cholangitis Gene Set

Cholangiocarcinoma in primary sclerosing cholangitis (time to event) Gene Set

Colorectal carcinoma in primary sclerosing cholangitis Gene Set

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Gene Set

Ichthyosis follicularis-alopecia-photophobia syndrome 1 Gene Set

Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa Of Siemens-Like Gene Set

vacuoles Gene Set

autophagic vacuoles Gene Set

rimmed vacuoles Gene Set

brain vacuoles Gene Set

muscular dystrophy with rimmed vacuoles Gene Set

Rimmed Vacuoles On Biopsy Gene Set

brain vacuoles Gene Set

Distal myopathy with rimmed vacuoles Gene Set

Rimmed vacuoles Gene Set

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene Set

Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

alopecia and lumbar herniated disk Gene Set

macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set

t-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene Set

T-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

T-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set

Palmoplantar keratoderma and congenital alopecia 2 Gene Set

Palmoplantar keratoderma and congenital alopecia 1 Gene Set

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set