cleft palate, isolated

Clear Filter

Results for "cleft palate, isolated": 583 gene sets

Name
cleft palate, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the cleft palate, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
cleft lip with cleft palate; cleft lip without cleft palate; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with cleft palate; cleft lip without cleft palate; cleft lip Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with or without cleft palate; cleft palate, isolated Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with or without cleft palate; cleft palate, isolated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set From GAD Gene-Disease Associations genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip without cleft palate; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Cleft Palate, Isolated, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cleft Palate, Isolated, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
hypothyroidism; cleft palate, isolated; thyroid agenesis Gene Set From GAD Gene-Disease Associations genes associated with the disease hypothyroidism; cleft palate, isolated; thyroid agenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Isolated cleft palate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated cleft palate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated cleft palate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with or without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonsyndromic cleft lipor without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease nonsyndromic cleft lipor without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypodontia; cleft lip; cleft palate; genetic diseases, inborn Gene Set From GAD Gene-Disease Associations genes associated with the disease hypodontia; cleft lip; cleft palate; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital anomalies; cleft lip with or without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital anomalies; cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; mouth abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; mouth abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; tooth abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; tooth abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, drug-induced; cleft lip; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, drug-induced; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate; cleft lip Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate; cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonsyndromic cleft lip with or without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease nonsyndromic cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome breakage; cleft lip; cleft palate; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome breakage; cleft lip; cleft palate; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; ectodermal dysplasia; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; ectodermal dysplasia; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Cleft Lip With Or Without Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Lip With Or Without Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonsyndromic Cleft Lip With Or Without Cleft Palate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonsyndromic Cleft Lip With Or Without Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Lip +/- Cleft Palate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cleft Lip +/- Cleft Palate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonsyndromic cleft lip with cleft palate Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nonsyndromic cleft lip with cleft palate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Nonsyndromic cleft lip with or without cleft palate Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nonsyndromic cleft lip with or without cleft palate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate x maternal periconceptional smoking interaction (parent of origin effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional smoking interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Nonsyndromic cleft lip with or without cleft palate x sex interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nonsyndromic cleft lip with or without cleft palate x sex interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
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.
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.
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.
Cleft palate with ankyloglossia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cleft palate with ankyloglossia 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.
Cleft Palate Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cleft Palate from the curated CTD Gene-Disease Associations dataset.
Microtia, Hearing Impairment, And Cleft Palate Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.
Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly-cleft lip/palate syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly-cleft lip/palate syndrome from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Cleft palate X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cleft palate X-linked from the curated CTD Gene-Disease Associations dataset.
Ankyloblepharon filiforme adnatum cleft palate Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ankyloblepharon filiforme adnatum cleft palate from the curated CTD Gene-Disease Associations dataset.
Cleft Palate Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Cleft Palate in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
cleft palate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cleft palate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cleft palate; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip and palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip and palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
non-syndromic cleft lip and palate Gene Set From GAD Gene-Disease Associations genes associated with the disease non-syndromic cleft lip and palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate and calvaria defects. Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate and calvaria defects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate; hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate; tongue diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate; tongue diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft soft palate Gene Set From HPO Gene-Disease Associations genes associated with the cleft soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
submucous cleft soft palate Gene Set From HPO Gene-Disease Associations genes associated with the submucous cleft soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft palate Gene Set From HPO Gene-Disease Associations genes associated with the cleft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral cleft lip and palate Gene Set From HPO Gene-Disease Associations genes associated with the bilateral cleft lip and palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral cleft palate Gene Set From HPO Gene-Disease Associations genes associated with the bilateral cleft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
non-midline cleft palate Gene Set From HPO Gene-Disease Associations genes associated with the non-midline cleft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
median cleft palate Gene Set From HPO Gene-Disease Associations genes associated with the median cleft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft hard palate Gene Set From HPO Gene-Disease Associations genes associated with the cleft hard palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
median cleft lip and palate Gene Set From HPO Gene-Disease Associations genes associated with the median cleft lip and palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
unilateral cleft palate Gene Set From HPO Gene-Disease Associations genes associated with the unilateral cleft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft secondary palate Gene Set From HPO Gene-Disease Associations genes associated with the cleft secondary palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
submucous cleft hard palate Gene Set From HPO Gene-Disease Associations genes associated with the submucous cleft hard palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cleft Palate Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cleft Palate phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cleft lip and palate transmembrane 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cleft lip and palate transmembrane 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cleft lip and palate transmembrane protein 1-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cleft lip and palate transmembrane protein 1-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
cleft palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cleft palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cleft primary palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cleft primary palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cleft secondary palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cleft secondary palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
submucous cleft palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the submucous cleft palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
?microtia, hearing impairment, and cleft palate (ar) Gene Set From OMIM Gene-Disease Associations genes associated with the ?microtia, hearing impairment, and cleft palate (ar) phenotype from the curated OMIM Gene-Disease Associations dataset.
cleft lip/palate-ectodermal dysplasia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cleft lip/palate-ectodermal dysplasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
cleft palate with ankyloglossia Gene Set From OMIM Gene-Disease Associations genes associated with the cleft palate with ankyloglossia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
acromegaloid features, overgrowth, cleft palate, and hernia Gene Set From OMIM Gene-Disease Associations genes associated with the acromegaloid features, overgrowth, cleft palate, and hernia phenotype from the curated OMIM Gene-Disease Associations dataset.
gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene Set From OMIM Gene-Disease Associations genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset.
coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Submucous Cleft Of Hard Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Submucous Cleft Of Hard Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Median Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Median Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unilateral Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unilateral Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Palate-Lateral Synechia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Palate-Lateral Synechia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Soft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Soft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Submucous Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Submucous Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Submucous Cleft Soft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Submucous Cleft Soft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Palate With Ankyloglossia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Palate With Ankyloglossia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Median Cleft Lip And Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Median Cleft Lip And Palate 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.
Ankyloblepharon Filiforme Adnatum And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ankyloblepharon Filiforme Adnatum And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Holoprosencephaly, Ectrodactyly, And Bilateral Cleft Lip-Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Holoprosencephaly, Ectrodactyly, And Bilateral Cleft Lip-Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hydronephrosis, Congenital, With Cleft Palate, Characteristic Facies, Hypotonia, And Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hydronephrosis, Congenital, With Cleft Palate, Characteristic Facies, Hypotonia, And Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia, Hearing Impairment, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia, Hearing Impairment, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Palate Alone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Palate Alone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Malformation, Cleft Lip-Palate, Microcephaly And Digital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Malformation, Cleft Lip-Palate, Microcephaly And Digital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coloboma, Cleft Lip-Palate And Mental Retardation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coloboma, Cleft Lip-Palate And Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Cleft Palate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bilateral Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Palate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft secondary palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft secondary palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft primary palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft primary palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
median cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the median cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bilateral cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bilateral cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
unilateral cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unilateral cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
complete cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the complete cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anterior cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft hard palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft hard palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
submucous cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the submucous cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft soft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft soft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft palate Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the cleft palate phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease ankyloblepharon-ectodermal defects-cleft lip/palate syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cleft palate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cleft palate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ankyloblepharon-ectodermal defects-cleft lip/palate syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft palate-lateral synechia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cleft palate-lateral synechia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft lip-palate-ectodermal dysplasia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cleft lip-palate-ectodermal dysplasia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft soft palate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cleft soft palate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked cleft palate with or without ankyloglossia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked cleft palate with or without ankyloglossia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Uveal coloboma-cleft lip and palate-intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uveal coloboma-cleft lip and palate-intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft palate, cardiac defects, and intellectual disabillity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cleft palate, cardiac defects, and intellectual disabillity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft palate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cholestasis-pigmentary retinopathy-cleft palate syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cholestasis-pigmentary retinopathy-cleft palate syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cleft lip/palate-ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cleft lip/palate-ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bilateral microtia-deafness-cleft palate syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bilateral microtia-deafness-cleft palate syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bilateral cleft palate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bilateral cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Uveal coloboma-cleft lip and palate-intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Uveal coloboma-cleft lip and palate-intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonsyndromic cleft palate Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nonsyndromic cleft palate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft palate Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft palate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
hard palate cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hard palate cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
soft palate cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease soft palate cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
palate Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term palate in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
PAX3_Knock-in_GDS3331_598_mouse_Palatal shelves (E14.5 embryos - palate) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PAX3_Knock-in_GDS3331_598_mouse_Palatal shelves (E14.5 embryos - palate) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
soft palate development Gene Set From GO Biological Process Annotations 2015 genes participating in the soft palate development biological process from the curated GO Biological Process Annotations 2015 dataset.
hard palate development Gene Set From GO Biological Process Annotations 2015 genes participating in the hard palate development biological process from the curated GO Biological Process Annotations 2015 dataset.
palate development Gene Set From GO Biological Process Annotations 2015 genes participating in the palate development biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormality of the soft palate Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the palate Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
high palate Gene Set From HPO Gene-Disease Associations genes associated with the high palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
high, narrow palate Gene Set From HPO Gene-Disease Associations genes associated with the high, narrow palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
palate telangiectasia Gene Set From HPO Gene-Disease Associations genes associated with the palate telangiectasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short hard palate Gene Set From HPO Gene-Disease Associations genes associated with the short hard palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
narrow palate Gene Set From HPO Gene-Disease Associations genes associated with the narrow palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the hard palate Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the hard palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent hard palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent hard palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary palate development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
high palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the high palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal primary palate development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal primary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal soft palate morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal soft palate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal palate bone morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal palate bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hard palate morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hard palate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
palate bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the palate bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal palate development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal palate morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal palate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
arched palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the arched palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
palate Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue palate in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Byzanthine Arch Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Byzanthine Arch Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Palate Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Palate Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Soft Palate Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Soft Palate Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Malformations Of Palate, Not Elsewhere Classified In Icd10Cm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformations Of Palate, Not Elsewhere Classified In Icd10Cm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Hard Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Hard Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hard Palate Squamous Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hard Palate Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
High, Narrow Palate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype High, Narrow Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Palate Telangiectasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Palate Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Narrow Palate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Palate Fistula Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Palate Fistula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Residue On Palate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Residue On Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
secondary palate development Gene Set From GO Biological Process Annotations 2023 genes participating in the secondary palate development biological process from the curated GO Biological Process Annotations 2023 dataset.
PRDM16-22522345-PALATE-MESENCHYMAL-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the PRDM16-22522345-PALATE-MESENCHYMAL-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
abnormal palate morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal palate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent soft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent soft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal secondary palate development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary palate development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal soft palate morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal soft palate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hard palate morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hard palate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent hard palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hard palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent primary palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent primary palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal palate development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal palate development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short soft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short soft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal palate bone morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal palate bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
palate bone hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the palate bone hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
arched palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the arched palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent palate bones Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent palate bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
high palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the high palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal secondary palate morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary palate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
narrow palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the narrow palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
secondary palate development Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary palate development biological process from the curated GO Biological Process Annotations 2025 dataset.
Hard palate cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hard palate cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Soft palate cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Soft palate cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Palate Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Palate in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
High palate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the High palate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated 17,20-lyase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Isolated 17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectopia lentis, isolated autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectopia lentis, isolated autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant isolated somatotropin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Isolated growth hormone deficiency type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Isolated growth hormone deficiency type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sulfite oxidase deficiency, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sulfite oxidase deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Follicle-stimulating hormone deficiency, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Follicle-stimulating hormone deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Laron-type isolated somatotropin defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperchlorhidrosis, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperchlorhidrosis, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital clubbing, isolated congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital clubbing, isolated congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated, with coloboma 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated, with coloboma 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated, with coloboma 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated, with coloboma 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microphthalmia, isolated, with coloboma 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microphthalmia, isolated, with coloboma 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mineralocorticoid deficiency, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Question mark ears, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Question mark ears, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectopia lentis, isolated, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectopia lentis, isolated, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
H2AX complex, isolated from cells without IR exposure Gene Set From CORUM Protein Complexes proteins in the H2AX complex, isolated from cells without IR exposure protein complex from the CORUM Protein Complexes dataset.
MICROPHTHALMIA, ISOLATED 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROPHTHALMIA, ISOLATED 5 from the curated CTD Gene-Disease Associations dataset.
MICROPHTHALMIA, ISOLATED 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROPHTHALMIA, ISOLATED 7 from the curated CTD Gene-Disease Associations dataset.
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6 from the curated CTD Gene-Disease Associations dataset.
Isolated Growth Hormone Deficiency, Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type II from the curated CTD Gene-Disease Associations dataset.
Hypoparathyroidism familial isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset.
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Coloboma 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 2 from the curated CTD Gene-Disease Associations dataset.
Isolated Growth Hormone Deficiency, Type IB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type IB from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Coloboma 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 5 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated 1 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated 3 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated 4 from the curated CTD Gene-Disease Associations dataset.
ACTH Deficiency, Isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ACTH Deficiency, Isolated from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated 2 from the curated CTD Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toenail Dystrophy, Isolated from the curated CTD Gene-Disease Associations dataset.
Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.
Hemihyperplasia, Isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemihyperplasia, Isolated from the curated CTD Gene-Disease Associations dataset.
HYPERCHLORHIDROSIS, ISOLATED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHLORHIDROSIS, ISOLATED from the curated CTD Gene-Disease Associations dataset.
ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset.
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Nail dysplasia, isolated congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nail dysplasia, isolated congenital from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Cataract 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 2 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Cataract 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 1 from the curated CTD Gene-Disease Associations dataset.
ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset.
Follicle-stimulating hormone deficiency, isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Follicle-stimulating hormone deficiency, isolated from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Coloboma 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 3 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Coloboma 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 1 from the curated CTD Gene-Disease Associations dataset.
isolated colobomas or colobomas associated Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated colobomas or colobomas associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
isolated gh deficiency (ighd) Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated gh deficiency (ighd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
isolated penile hypospadias Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated penile hypospadias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
isolated Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term isolated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
microphthalmia, isolated 8 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated 1 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated 3 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated 2 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated 5 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated 4 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated 7 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated 6 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia with isolated vitamin e deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia with isolated vitamin e deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?isolated growth hormone deficiency due to defect in ghrf Gene Set From OMIM Gene-Disease Associations genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
ectopia lentis, isolated, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ectopia lentis, isolated, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
agammaglobulinemia and isolated hormone deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the agammaglobulinemia and isolated hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, with isolated growth hormone deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, with isolated growth hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated, with coloboma 7 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated, with coloboma 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated, with coloboma 8 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated, with coloboma 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia, isolated, with coloboma 9 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia, isolated, with coloboma 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
toenail dystrophy, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the toenail dystrophy, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
preauricular tag, isolated, autosomal dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the preauricular tag, isolated, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
asplenia, isolated congenital Gene Set From OMIM Gene-Disease Associations genes associated with the asplenia, isolated congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
giant platelet disorder, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the giant platelet disorder, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoparathyroidism, familial isolated Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism, familial isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
17,20-lyase deficiency, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the 17,20-lyase deficiency, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
myelokathexis, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the myelokathexis, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
growth hormone deficiency, isolated, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the growth hormone deficiency, isolated, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
growth hormone deficiency, isolated, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the growth hormone deficiency, isolated, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
growth hormone deficiency, isolated, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the growth hormone deficiency, isolated, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
renal hypoplasia, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the renal hypoplasia, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
follicle-stimulating hormone deficiency, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the follicle-stimulating hormone deficiency, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
invasive pneumococcal disease, recurrent isolated, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
invasive pneumococcal disease, recurrent isolated, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperchlorhidrosis, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the hyperchlorhidrosis, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
digital clubbing, isolated congenital Gene Set From OMIM Gene-Disease Associations genes associated with the digital clubbing, isolated congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
question mark ears, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the question mark ears, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
anosmia, isolated congenital Gene Set From OMIM Gene-Disease Associations genes associated with the anosmia, isolated congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
Scoliosis, Isolated, Susceptibility To, 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scoliosis, Isolated, Susceptibility To, 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Systolic Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Systolic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Somatotropin Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Somatotropin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemihyperplasia, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemihyperplasia, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Cystinuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Cystinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Melorheostosis, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Melorheostosis, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Polycystic Liver Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Polycystic Liver Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Clinically Isolated Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Clinically Isolated Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Cervical Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Cervical Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Atp Synthase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Atp Synthase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Hypoplasia Of The Right Ventricle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Hypoplasia Of The Right Ventricle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Follicle-Stimulating Hormone Deficiency, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Follicle-Stimulating Hormone Deficiency, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Isolated Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Radiologically Isolated Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Radiologically Isolated Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acth Deficiency, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acth Deficiency, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toenail Dystrophy, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Deficiency Of Pituitary Hormone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Deficiency Of Pituitary Hormone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Gonadotropin Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Gonadotropin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Growh Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Growh Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Growth Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Growth Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Lutropin Deficiency (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Lutropin Deficiency (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myelokathexis, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myelokathexis, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
17,20-Lyase Deficiency, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 17,20-Lyase Deficiency, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Question Mark Ears, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Question Mark Ears, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Isolated Trichomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Trichomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptophthalmos, Unilateral Or Bilateral, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptophthalmos, Unilateral Or Bilateral, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Cryptophthalmos Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Cryptophthalmos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anhidrosis, Isolated, With Normal Sweat Glands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anhidrosis, Isolated, With Normal Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Bone Marrow Mastocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Bone Marrow Mastocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dermatofibrosis Lenticularis Disseminata, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dermatofibrosis Lenticularis Disseminata, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteopoikilosis, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteopoikilosis, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rare Isolated Myopia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rare Isolated Myopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Natural Killer Cell Deficiency, Familial Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Natural Killer Cell Deficiency, Familial Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Aortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Atrial Amyloid Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Atrial Amyloid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Blepharospasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Blepharospasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Foveal Hypoplasia, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Foveal Hypoplasia, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Caroli Disease Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Caroli Disease Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Isolated Thyroid Stimulating Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Isolated Thyroid Stimulating Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Isolated Adrenocorticotropic Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Isolated Adrenocorticotropic Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Focal Cortical Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Focal Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyrotropin Deficiency, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyrotropin Deficiency, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Cases Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Isolated Cases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Isolated Hyperchlorhidrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Isolated Hyperchlorhidrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Isolated Asymptomatic Elevation Of Creatine Phosphokinase Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Isolated Asymptomatic Elevation Of Creatine Phosphokinase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Prolactin Deficiency, Isolated Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolactin Deficiency, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Isolated sulfite oxidase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Isolated sulfite oxidase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial isolated deficiency of vitamin E Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial isolated deficiency of vitamin E from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Isolated growth hormone deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Isolated growth hormone deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Isolated hyperchlorhidrosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Isolated hyperchlorhidrosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Isolated elevated serum creatine phosphokinase levels Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Isolated elevated serum creatine phosphokinase levels from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Isolated ectopia lentis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Isolated ectopia lentis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Isolated microphthalmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated microphthalmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated hyperchlorhidrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated hyperchlorhidrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial isolated hypoparathyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial isolated hypoparathyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated growth hormone deficiency type IA Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated growth hormone deficiency type IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated growth hormone deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated growth hormone deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial isolated deficiency of vitamin E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial isolated deficiency of vitamin E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated ectopia lentis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated ectopia lentis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated growth hormone deficiency type IB Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated growth hormone deficiency type IB in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial isolated trichomegaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial isolated trichomegaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated microphthalmia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated microphthalmia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated sulfite oxidase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated sulfite oxidase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated growth hormone deficiency type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated growth hormone deficiency type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated elevated serum creatine phosphokinase levels Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated elevated serum creatine phosphokinase levels in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated microphthalmia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated microphthalmia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated anhidrosis with normal sweat glands Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated anhidrosis with normal sweat glands in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated cryptophthalmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated cryptophthalmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated microphthalmia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated microphthalmia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated microphthalmia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated microphthalmia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated growth hormone deficiency type III Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated growth hormone deficiency type III in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated microphthalmia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated microphthalmia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive isolated ectopia lentis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive isolated ectopia lentis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant isolated ectopia lentis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant isolated ectopia lentis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated microphthalmia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated microphthalmia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial isolated arrhythmogenic right ventricular dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated arrhythmogenic right ventricular dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated optic nerve hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated optic nerve hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated microphthalmia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated microphthalmia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated focal cortical dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated focal cortical dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital isolated adrenocorticotropic hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital isolated adrenocorticotropic hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated congenital digital clubbing Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated congenital digital clubbing phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial isolated deficiency of vitamin Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated deficiency of vitamin phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial isolated dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated thyroid-stimulating hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated thyroid-stimulating hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated lutropin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated lutropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant isolated somatotropin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated growth hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated congenital hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated congenital hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated GnRH Deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated GnRH Deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated thoracic aortic aneurysm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial isolated pituitary adenoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated pituitary adenoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated Nonsyndromic Congenital Heart disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated Nonsyndromic Congenital Heart disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated systolic hypertension Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated systolic hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated Coronal Synostosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated Coronal Synostosis phenotype from the curated ClinVar Gene-Phenotype Associations 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.
Isolated focal non-epidermolytic palmoplantar keratoderma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated focal non-epidermolytic palmoplantar keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated cryptophthalmia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated cryptophthalmia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated Noncompaction of the Ventricular Myocardium Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated Noncompaction of the Ventricular Myocardium phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated Pierre-Robin syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated Pierre-Robin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated Hyperparathyroidism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated Hyperparathyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated congenital growth hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated congenital growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial isolated congenital asplenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated congenital asplenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated anophthalmia-microphthalmia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated anophthalmia-microphthalmia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated agenesis of gallbladder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated agenesis of gallbladder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated hereditary giant platelet disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated hereditary giant platelet disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial isolated hyperparathyroidism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated hyperparathyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated anhidrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated anhidrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated hyperchlorhidrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated hyperchlorhidrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated ectopia lentis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated ectopia lentis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated sedoheptulokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated sedoheptulokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rare isolated myopia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare isolated myopia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Orofacial cleft 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofacial cleft 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Orofacial cleft 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofacial cleft 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Orofacial cleft 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofacial cleft 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
synaptic cleft Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the synaptic cleft cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
synaptic cleft Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the synaptic cleft cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Orofacial Cleft 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 9 from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 1 from the curated CTD Gene-Disease Associations dataset.
Cleft Lip Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cleft Lip from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 4 from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 2 from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 5 from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 3 from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 12 from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 10 from the curated CTD Gene-Disease Associations dataset.
Orofacial Cleft 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofacial Cleft 11 from the curated CTD Gene-Disease Associations dataset.
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OROFACIAL CLEFT 6, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Cleft Lip Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Cleft Lip in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
orofacial cleft Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease orofacial cleft in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
orofacial cleft Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease orofacial cleft in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cleft lip Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cleft lip in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
non-syndromic cleft lip Gene Set From GAD Gene-Disease Associations genes associated with the disease non-syndromic cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonsymdromic cleft lip Gene Set From GAD Gene-Disease Associations genes associated with the disease nonsymdromic cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonsyndromic cleft lip Gene Set From GAD Gene-Disease Associations genes associated with the disease nonsyndromic cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cleft in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
acetylcholine catabolic process in synaptic cleft Gene Set From GO Biological Process Annotations 2015 genes participating in the acetylcholine catabolic process in synaptic cleft biological process from the curated GO Biological Process Annotations 2015 dataset.
synaptic cleft Gene Set From GO Cellular Component Annotations 2015 proteins localized to the synaptic cleft cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Cleft plate (environmental tobacco smoke interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cleft plate (environmental tobacco smoke interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
cleft lip Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cleft lip in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
orofacial cleft Gene Set From GWASdb SNP-Disease Associations genes associated with the disease orofacial cleft in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
oral cleft Gene Set From GWASdb SNP-Phenotype Associations genes associated with the oral cleft phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cleft ala nasi Gene Set From HPO Gene-Disease Associations genes associated with the cleft ala nasi phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
unilateral cleft lip Gene Set From HPO Gene-Disease Associations genes associated with the unilateral cleft lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft upper lip Gene Set From HPO Gene-Disease Associations genes associated with the cleft upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
non-midline cleft lip Gene Set From HPO Gene-Disease Associations genes associated with the non-midline cleft lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft vertebral arch Gene Set From HPO Gene-Disease Associations genes associated with the cleft vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
submucous cleft lip Gene Set From HPO Gene-Disease Associations genes associated with the submucous cleft lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft eyelid Gene Set From HPO Gene-Disease Associations genes associated with the cleft eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midline facial cleft Gene Set From HPO Gene-Disease Associations genes associated with the midline facial cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
median cleft lip Gene Set From HPO Gene-Disease Associations genes associated with the median cleft lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft in skull base Gene Set From HPO Gene-Disease Associations genes associated with the cleft in skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
oral cleft Gene Set From HPO Gene-Disease Associations genes associated with the oral cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft at the superior portion of the pinna Gene Set From HPO Gene-Disease Associations genes associated with the cleft at the superior portion of the pinna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft of chin Gene Set From HPO Gene-Disease Associations genes associated with the cleft of chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft lower alveolar ridge Gene Set From HPO Gene-Disease Associations genes associated with the cleft lower alveolar ridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft helix Gene Set From HPO Gene-Disease Associations genes associated with the cleft helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
facial cleft Gene Set From HPO Gene-Disease Associations genes associated with the facial cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
coronal cleft vertebrae Gene Set From HPO Gene-Disease Associations genes associated with the coronal cleft vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft mandible Gene Set From HPO Gene-Disease Associations genes associated with the cleft mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior pharyngeal cleft Gene Set From HPO Gene-Disease Associations genes associated with the posterior pharyngeal cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
laryngeal cleft Gene Set From HPO Gene-Disease Associations genes associated with the laryngeal cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral cleft lip Gene Set From HPO Gene-Disease Associations genes associated with the bilateral cleft lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
alveolar ridge cleft Gene Set From HPO Gene-Disease Associations genes associated with the alveolar ridge cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cleft Lip Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cleft Lip phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
midline facial cleft Gene Set From MPO Gene-Phenotype Associations gene mutations causing the midline facial cleft phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cleft lip Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cleft lip phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cleft chin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cleft chin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oblique facial cleft Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oblique facial cleft phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
facial cleft Gene Set From MPO Gene-Phenotype Associations gene mutations causing the facial cleft phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
orofacial cleft 9 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 8 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 7 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 6 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 5 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 4 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
robin sequence with cleft mandible and limb anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the robin sequence with cleft mandible and limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 13 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft-1 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft-2 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft-3 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 14 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 12 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 11 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
orofacial cleft 10 Gene Set From OMIM Gene-Disease Associations genes associated with the orofacial cleft 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, 1, with or without orofacial cleft Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, 1, with or without orofacial cleft phenotype from the curated OMIM Gene-Disease Associations dataset.
Neurotransmitter Clearance In The Synaptic Cleft Gene Set From Reactome Pathways 2014 proteins participating in the Neurotransmitter Clearance In The Synaptic Cleft pathway from the Reactome Pathways dataset.
Serotonin clearance from the synaptic cleft Gene Set From Reactome Pathways 2014 proteins participating in the Serotonin clearance from the synaptic cleft pathway from the Reactome Pathways dataset.
Dopamine clearance from the synaptic cleft Gene Set From Reactome Pathways 2014 proteins participating in the Dopamine clearance from the synaptic cleft pathway from the Reactome Pathways dataset.
Neurotransmitter Clearance In The Synaptic Cleft(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Neurotransmitter Clearance In The Synaptic Cleft(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Cleft Lip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oral Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oral Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Orofacial Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Orofacial Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngeal Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Laryngeal Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Midline Cervical Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Midline Cervical Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Face Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Face in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Midline Facial Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Midline Facial Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Median Cleft Lip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Median Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypodontia Oligodontia With Orofacial Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypodontia Oligodontia With Orofacial Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fistula Of Branchial Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fistula Of Branchial Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Lip, Congenital Healed Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Lip, Congenital Healed in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rathke Cleft Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rathke Cleft Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unilateral Cleft Lip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unilateral Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Earlobe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Earlobe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sternal Cleft Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sternal Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Midline Cleft Lip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Midline Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Cleft Lip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Uvula Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Uvula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unilateral Alveolar Cleft Of Maxilla Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unilateral Alveolar Cleft Of Maxilla in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Leaflet Of Mitral Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Leaflet Of Mitral Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Lip Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Anterior Mitral Valve Leaflet Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Anterior Mitral Valve Leaflet in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Pharyngeal Cleft Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Pharyngeal Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Coronal Cleft Vertebrae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Coronal Cleft Vertebrae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Helix Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Helix in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Lower Alveolar Ridge Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Lower Alveolar Ridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Mandible Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Mandible in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Of Chin Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Of Chin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Ala Nasi Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Ala Nasi in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft At The Superior Portion Of The Pinna Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft At The Superior Portion Of The Pinna in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Submucous Cleft Lip Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Submucous Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft In Skull Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft In Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gingival Cleft Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gingival Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft Alveolar Process Of Maxilla Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Alveolar Process Of Maxilla in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
acetylcholine catabolic process in synaptic cleft Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine catabolic process in synaptic cleft biological process from the curated GO Biological Process Annotations 2023 dataset.
cleft chin Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft chin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
midline facial cleft Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the midline facial cleft phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
unilateral cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unilateral cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bilateral cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bilateral cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
facial cleft Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the facial cleft phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
midline cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the midline cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
oblique facial cleft Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the oblique facial cleft phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
oral cleft Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the oral cleft phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
facial cleft Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the facial cleft phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
synaptic cleft Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term synaptic cleft from the SynGO Synaptic Gene Annotations dataset.
extracellular matrix of synaptic cleft Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term extracellular matrix of synaptic cleft from the SynGO Synaptic Gene Annotations dataset.
Dopamine clearance from the synaptic cleft Gene Set From Reactome Pathways 2024 proteins participating in the Dopamine clearance from the synaptic cleft pathway from the Reactome Pathways 2024 dataset.
Serotonin clearance from the synaptic cleft Gene Set From Reactome Pathways 2024 proteins participating in the Serotonin clearance from the synaptic cleft pathway from the Reactome Pathways 2024 dataset.
acetylcholine catabolic process in synaptic cleft Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine catabolic process in synaptic cleft biological process from the curated GO Biological Process Annotations 2025 dataset.
Orofacial cleft Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Orofacial cleft in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft lip Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cleft lip in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft lip Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cleft lip in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Orofacial cleft 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orofacial cleft 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Synaptic cleft Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Synaptic cleft cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Synaptic cleft Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Synaptic cleft cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Extracellular matrix of synaptic cleft Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Extracellular matrix of synaptic cleft cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Orofacial cleft Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Orofacial cleft phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Branchial cleft anomaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Branchial cleft anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cleft lip Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cleft lip phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Midline facial cleft Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Midline facial cleft phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cleft plate (environmental tobacco smoke interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft plate (environmental tobacco smoke interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Nonsyndromic cleft lip Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nonsyndromic cleft lip phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Orofacial cleft x maternal periconceptional smoking interaction (1df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional smoking interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Orofacial cleft x maternal periconceptional alcohol use interaction (1df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional alcohol use interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Orofacial cleft x maternal periconceptional multivitamin use interaction (1df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional multivitamin use interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Orofacial cleft x maternal periconceptional smoking interaction (2df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional smoking interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Orofacial cleft x maternal periconceptional alcohol use interaction (2df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional alcohol use interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Orofacial cleft x maternal periconceptional multivitamin use interaction (2df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional multivitamin use interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

cleft palate, isolated Gene Set

cleft lip with cleft palate; cleft lip without cleft palate; cleft palate Gene Set

cleft lip with cleft palate; cleft lip without cleft palate; cleft lip Gene Set

cleft lip with or without cleft palate; cleft palate, isolated Gene Set

hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

cleft lip with cleft palate; cleft lip without cleft palate Gene Set

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

cleft lip without cleft palate; cleft palate Gene Set

Cleft Palate, Isolated, And Mental Retardation Gene Set

hypothyroidism; cleft palate, isolated; thyroid agenesis Gene Set

Isolated cleft palate Gene Set

Isolated cleft palate Gene Set

cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic Gene Set

cleft lip; cleft palate; syndrome Gene Set

cleft lip; cleft palate; Gene Set

chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set

cleft lip; cleft palate; congenital abnormalities Gene Set

cleft lip with or without cleft palate Gene Set

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

nonsyndromic cleft lipor without cleft palate Gene Set

hypodontia; cleft lip; cleft palate; genetic diseases, inborn Gene Set

cleft lip; cleft palate; prenatal exposure delayed effects Gene Set

congenital anomalies; cleft lip with or without cleft palate Gene Set

cleft lip; cleft palate; mouth abnormalities Gene Set

cleft lip; cleft palate; tooth abnormalities Gene Set

cleft lip; cleft palate Gene Set

abnormalities, drug-induced; cleft lip; cleft palate Gene Set

cleft palate; cleft lip Gene Set

nonsyndromic cleft lip with or without cleft palate Gene Set

chromosome breakage; cleft lip; cleft palate; translocation, genetic Gene Set

cleft lip; cleft palate; ectodermal dysplasia; syndrome Gene Set

Cleft Lip With Or Without Cleft Palate Gene Set

Nonsyndromic Cleft Lip With Or Without Cleft Palate Gene Set

Cleft Lip +/- Cleft Palate Gene Set

Nonsyndromic cleft lip with cleft palate Gene Set

Nonsyndromic cleft lip with or without cleft palate Gene Set

Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) Gene Set

Cleft lip with or without cleft palate x maternal periconceptional smoking interaction (parent of origin effect) Gene Set

Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) Gene Set

Nonsyndromic cleft lip with or without cleft palate x sex interaction (2df test) Gene Set

Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) Gene Set

Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) Gene Set

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

Microtia, hearing impairment, and cleft palate Gene Set

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

Cleft palate with ankyloglossia Gene Set

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

Cleft Palate Gene Set

Microtia, Hearing Impairment, And Cleft Palate Gene Set

Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set

Ectrodactyly-cleft lip/palate syndrome Gene Set

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set

Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set

Cleft palate X-linked Gene Set

Ankyloblepharon filiforme adnatum cleft palate Gene Set

Cleft Palate Gene Set

cleft palate Gene Set

cleft palate; syndrome Gene Set

cleft lip and palate Gene Set

non-syndromic cleft lip and palate Gene Set

cleft palate and calvaria defects. Gene Set

cleft palate Gene Set

cleft palate; hypothyroidism Gene Set

cleft palate; prenatal exposure delayed effects Gene Set

cleft palate; tongue diseases Gene Set

cleft soft palate Gene Set

submucous cleft soft palate Gene Set

cleft palate Gene Set

bilateral cleft lip and palate Gene Set

bilateral cleft palate Gene Set

non-midline cleft palate Gene Set

median cleft palate Gene Set

cleft hard palate Gene Set

median cleft lip and palate Gene Set

unilateral cleft palate Gene Set