Dentinogenesis Imperfecta Without Osteogenesis Imperfecta

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Results for "Dentinogenesis Imperfecta Without Osteogenesis Imperfecta": 468 gene sets

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Dentinogenesis Imperfecta Without Osteogenesis Imperfecta Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentinogenesis Imperfecta Without Osteogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentinogenesis imperfecta - Shield's type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dentinogenesis imperfecta - Shield's type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 from the curated CTD Gene-Disease Associations dataset.
Dentinogenesis Imperfecta Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dentinogenesis Imperfecta from the curated CTD Gene-Disease Associations dataset.
Dentinogenesis imperfecta, shields type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dentinogenesis imperfecta, shields type 3 from the curated CTD Gene-Disease Associations dataset.
dentinogenesis imperfecta Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dentinogenesis imperfecta from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dentinogenesis imperfecta Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentinogenesis imperfecta in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dentinogenesis imperfecta Gene Set From HPO Gene-Disease Associations genes associated with the dentinogenesis imperfecta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dentinogenesis imperfecta, shields type ii Gene Set From OMIM Gene-Disease Associations genes associated with the dentinogenesis imperfecta, shields type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
dentinogenesis imperfecta, shields type iii Gene Set From OMIM Gene-Disease Associations genes associated with the dentinogenesis imperfecta, shields type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
Dentinogenesis Imperfecta - Shield'S Type Iii (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentinogenesis Imperfecta - Shield'S Type Iii (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentinogenesis Imperfecta Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentinogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentinogenesis Imperfecta Limited To Primary Teeth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentinogenesis Imperfecta Limited To Primary Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentinogenesis imperfecta Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dentinogenesis imperfecta from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dentinogenesis imperfecta Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dentinogenesis imperfecta in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dentinogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dentinogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Osteogenesis imperfecta type 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta with normal sclerae, dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta with normal sclerae, dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta, recessive perinatal lethal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta, recessive perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta Levin type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta Levin type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
OSTEOGENESIS IMPERFECTA, TYPE IIC Gene Set From ClinVar Gene-Phenotype Associations genes associated with the OSTEOGENESIS IMPERFECTA, TYPE IIC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 2, thin-bone Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 2, thin-bone phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta type III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta, type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis imperfecta, type 2A from the curated CTD Gene-Disease Associations dataset.
Osteogenesis Imperfecta Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis Imperfecta from the curated CTD Gene-Disease Associations dataset.
Osteogenesis imperfecta, type 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis imperfecta, type 7 from the curated CTD Gene-Disease Associations dataset.
Osteogenesis imperfecta, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis imperfecta, type 3 from the curated CTD Gene-Disease Associations dataset.
Osteogenesis Imperfecta, Type IX Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis Imperfecta, Type IX from the curated CTD Gene-Disease Associations dataset.
Osteogenesis imperfecta, type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis imperfecta, type 4 from the curated CTD Gene-Disease Associations dataset.
Osteogenesis imperfecta, type VIII Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis imperfecta, type VIII from the curated CTD Gene-Disease Associations dataset.
osteogenesis imperfecta Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease osteogenesis imperfecta from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
osteogenesis imperfecta Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease osteogenesis imperfecta in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hearing loss/deafness; osteogenesis imperfecta Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing loss/deafness; osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild osteogenesis imperfecta Gene Set From GAD Gene-Disease Associations genes associated with the disease mild osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
osteogenesis imperfecta Gene Set From GAD Gene-Disease Associations genes associated with the disease osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Osteogenesis Imperfecta Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Osteogenesis Imperfecta phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
osteogenesis imperfecta, type vi Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type viii Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type viii phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type vii Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type vii phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type xi Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type xi phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type xv Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type xv phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type xiii Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type xiii phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type v Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type v phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type i Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type i phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type xiv Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type xiv phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type xii Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type xii phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type ix Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis imperfecta, type x Gene Set From OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type x phenotype from the curated OMIM Gene-Disease Associations dataset.
Osteogenesis Imperfecta Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteogenesis Imperfecta Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Type I collagen synthesis in the context of osteogenesis imperfecta Gene Set From WikiPathways Pathways 2024 proteins participating in the Type I collagen synthesis in the context of osteogenesis imperfecta pathway from the WikiPathways Pathways 2024 dataset.
Osteogenesis imperfecta Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Osteogenesis imperfecta from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta type 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteogenesis imperfecta type 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Osteogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined osteogenesis imperfecta and Ehlers-Danlos syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined osteogenesis imperfecta and Ehlers-Danlos syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
dentinogenesis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dentinogenesis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
dentinogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the dentinogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
deafness, autosomal dominant 36, with dentinogenesis Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 36, with dentinogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
osteogenesis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term osteogenesis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AMELOGENESIS IMPERFECTA, TYPE IH Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AMELOGENESIS IMPERFECTA, TYPE IH phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amelogenesis imperfecta, hypocalcification type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amelogenesis imperfecta, hypocalcification type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amelogenesis imperfecta pigmented hypomaturation type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amelogenesis imperfecta pigmented hypomaturation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amelogenesis imperfecta - hypoplastic autosomal dominant - local phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy amelogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amelogenesis Imperfecta, Type III Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis Imperfecta, Type III from the curated CTD Gene-Disease Associations dataset.
Amelogenesis Imperfecta Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis Imperfecta from the curated CTD Gene-Disease Associations dataset.
Amelogenesis Imperfecta, Type IV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis Imperfecta, Type IV from the curated CTD Gene-Disease Associations dataset.
Amelogenesis Imperfecta, Hypomaturation Type, Iia2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis Imperfecta, Hypomaturation Type, Iia2 from the curated CTD Gene-Disease Associations dataset.
Amelogenesis Imperfecta, Type Ic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis Imperfecta, Type Ic from the curated CTD Gene-Disease Associations dataset.
Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 from the curated CTD Gene-Disease Associations dataset.
Amelogenesis Imperfecta, Hypomaturation Type, Iia3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis Imperfecta, Hypomaturation Type, Iia3 from the curated CTD Gene-Disease Associations dataset.
Amelogenesis Imperfecta, Type IB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis Imperfecta, Type IB from the curated CTD Gene-Disease Associations dataset.
Amelogenesis imperfecta pigmented hypomaturation type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amelogenesis imperfecta pigmented hypomaturation type from the curated CTD Gene-Disease Associations dataset.
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 from the curated CTD Gene-Disease Associations dataset.
amelogenesis imperfecta Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease amelogenesis imperfecta from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
fibrogenesis imperfecta ossium Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fibrogenesis imperfecta ossium in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
amelogenesis imperfecta Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease amelogenesis imperfecta in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
imperfecta Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term imperfecta in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
amelogenesis imperfecta Gene Set From HPO Gene-Disease Associations genes associated with the amelogenesis imperfecta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
amelogenesis imperfecta, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type 1e Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type ig (enamel-renal syndrome) Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type ig (enamel-renal syndrome) phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type iia5 Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type iia5 phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type iia3 Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type iia3 phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type iia2 Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type iia2 phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type iia1 Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type iia1 phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta type, iia4 Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta type, iia4 phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
amelogenesis imperfecta, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the amelogenesis imperfecta, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
Amelogenesis Imperfecta Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amelogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Odontogenesis Imperfecta Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Odontogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomineralized Amelogenesis Imperfecta Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypomineralized Amelogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Amelogenesis Imperfecta Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Amelogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI) pathway from the Reactome Pathways 2024 dataset.
Amelogenesis imperfecta Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Amelogenesis imperfecta from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 1G Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 1G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 1E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 1E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 1C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 3A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta hypomaturation type 2A5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta hypomaturation type 2A5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 1J Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 1J in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
brachyolmia-amelogenesis imperfecta syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease brachyolmia-amelogenesis imperfecta syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fibrogenesis imperfecta ossium Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fibrogenesis imperfecta ossium in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta hypomaturation type 2A3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta hypomaturation type 2A3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta hypomaturation type 2A2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta hypomaturation type 2A2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta type 3C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amelogenesis imperfecta type 3C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Amelogenesis imperfecta hypomaturation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Amelogenesis imperfecta hypomaturation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Amelogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Amelogenesis imperfecta - hypoplastic autosomal dominant - local phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypomaturation-hypoplastic amelogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypomaturation-hypoplastic amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Brachyolmia-amelogenesis imperfecta syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Brachyolmia-amelogenesis imperfecta syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bronchiectasis with or without elevated sweat chloride 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 12 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy, cystic, without megalencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy, cystic, without megalencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cognitive impairment with or without cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 19 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 17 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bronchiectasis with or without elevated sweat chloride 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, without vestibular involvement, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, without vestibular involvement, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Testicular anomalies with or without congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Capillary malformation without arteriovenous malformation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acrodysostosis 2, with or without hormone resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acrodysostosis 2, with or without hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 13 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation, with or without seizures, ARX-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 10 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal epilepsy with speech disorder with or without mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 11 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
IFAP syndrome with or without BRESHECK syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency 26 with or without neurologic abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency 26 with or without neurologic abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness 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.
DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy, Cystic, Without Megalencephaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy, Cystic, Without Megalencephaly from the curated CTD Gene-Disease Associations dataset.
NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.
Migraine without Aura Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Migraine without Aura from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.
Bronchiectasis With Or Without Elevated Sweat Chloride 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 1 from the curated CTD Gene-Disease Associations dataset.
Bronchiectasis With Or Without Elevated Sweat Chloride 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 2 from the curated CTD Gene-Disease Associations dataset.
Bronchiectasis With Or Without Elevated Sweat Chloride 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 3 from the curated CTD Gene-Disease Associations dataset.
Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.
Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.
MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.
Metaphyseal Dysplasia without Hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.
Nonmedullary thyroid carcinoma, with or without cell oxyphilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nonmedullary thyroid carcinoma, with or without cell oxyphilia from the curated CTD Gene-Disease Associations dataset.
SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.
Migraine without Aura Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Migraine without Aura in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
migraine without aura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease migraine without aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 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.
salmeterol with or without fluticasone propionate Gene Set From GAD Gene-Disease Associations genes associated with the disease salmeterol with or without fluticasone propionate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; migraine with aura; migraine without aura; tension-type headache Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; migraine with aura; migraine without aura; tension-type headache 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.
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.
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.
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.
migraine without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine with aura; migraine without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine with aura; migraine without aura 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.
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.
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.
migraine with and without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine with and without aura 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.
migraine disorders; migraine with aura; migraine without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; migraine with aura; migraine without aura 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.
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.
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.
alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy 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.
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.
without Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term without in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2015 dataset.
Migraine without aura Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
migraine without aura Gene Set From GWASdb SNP-Disease Associations genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
migraine without aura Gene Set From GWASdb SNP-Phenotype Associations genes associated with the migraine without aura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal seizures without impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
migraine without aura Gene Set From HPO Gene-Disease Associations genes associated with the migraine without aura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Migraine without Aura Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Migraine without Aura phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypogonadotropic hypogonadism 15 with or without anosmia} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypogonadotropic hypogonadism 15 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
brain small vessel disease with or without ocular anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
paragangliomas 1, with or without deafness Gene Set From OMIM Gene-Disease Associations genes associated with the paragangliomas 1, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
metaphyseal dysplasia without hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 4 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set From OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 14 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 14 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
waardenburg syndrome, type 2e, with or without neurologic involvement Gene Set From OMIM Gene-Disease Associations genes associated with the waardenburg syndrome, type 2e, with or without neurologic involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
cognitive impairment with or without cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 6 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 10 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 3 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 3 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine without aura, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine without aura, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 8 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 8 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukemia, megakaryoblastic, with or without down syndrome, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the leukemia, megakaryoblastic, with or without down syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set From OMIM Gene-Disease Associations genes associated with the antley-bixler syndrome without genital anomalies or disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 5 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 5 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 7 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
?microtia with or without hearing impairment (ad) Gene Set From OMIM Gene-Disease Associations genes associated with the ?microtia with or without hearing impairment (ad) phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 11 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 18 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 18 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
{bronchiectasis with or without elevated sweat chloride 1, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {bronchiectasis with or without elevated sweat chloride 1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine, with or without aura, susceptibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine, with or without aura, susceptibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set From OMIM Gene-Disease Associations genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
?testicular anomalies with or without congenital heart disease Gene Set From OMIM Gene-Disease Associations genes associated with the ?testicular anomalies with or without congenital heart disease phenotype from the curated OMIM Gene-Disease Associations dataset.
dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema Gene Set From OMIM Gene-Disease Associations genes associated with the dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema phenotype from the curated OMIM Gene-Disease Associations dataset.
hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 2 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 2 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
bronchiectasis with or without elevated sweat chloride 1 Gene Set From OMIM Gene-Disease Associations genes associated with the bronchiectasis with or without elevated sweat chloride 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
bronchiectasis with or without elevated sweat chloride 2 Gene Set From OMIM Gene-Disease Associations genes associated with the bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
bronchiectasis with or without elevated sweat chloride 3 Gene Set From OMIM Gene-Disease Associations genes associated with the bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set From OMIM Gene-Disease Associations genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.
acrodysostosis 1, with or without hormone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the acrodysostosis 1, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 20 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 20 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
?hypogonadotropic hypogonadism 13 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the ?hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set From OMIM Gene-Disease Associations genes associated with the leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary hypertension, familial primary, 1, with or without hht Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
woolly hair, autosomal recessive 1, with or without hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 4 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 4 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, frontotemporal, with or without parkinsonism Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, frontotemporal, with or without parkinsonism phenotype from the curated OMIM Gene-Disease Associations dataset.
leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set From OMIM Gene-Disease Associations genes associated with the leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 9 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 9 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine without aura, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine without aura, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
left ventricular noncompaction 1, with or without congenital heart defects Gene Set From OMIM Gene-Disease Associations genes associated with the left ventricular noncompaction 1, with or without congenital heart defects 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.
{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
?hypogonadotropic hypogonadism 12 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the ?hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From OMIM Gene-Disease Associations genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 6 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 6 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 9, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 9, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract, pulverulent or cerulean, with or without microcornea Gene Set From OMIM Gene-Disease Associations genes associated with the cataract, pulverulent or cerulean, with or without microcornea phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set From OMIM Gene-Disease Associations genes associated with the noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated OMIM Gene-Disease Associations dataset.
retinitis pigmentosa with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the retinitis pigmentosa with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 7, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 7, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
gyrate atrophy of choroid and retina with or without ornithinemia Gene Set From OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 19 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine with or without aura, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine with or without aura, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, with or without nystagmus Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, neurosensory, without vestibular involvement, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, neurosensory, without vestibular involvement, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.
adult i phenotype without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, cystic, without megalencephaly Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, cystic, without megalencephaly phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine with or without aura, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine with or without aura, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 8 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
branchiootorenal syndrome 1, with or without cataracts Gene Set From OMIM Gene-Disease Associations genes associated with the branchiootorenal syndrome 1, with or without cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.
mcleod syndrome with or without chronic granulomatous disease Gene Set From OMIM Gene-Disease Associations genes associated with the mcleod syndrome with or without chronic granulomatous disease phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine with or without aura, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine with or without aura, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 1, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 1, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set From OMIM Gene-Disease Associations genes associated with the mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine, with or without aura, susceptibility to, 13} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine, with or without aura, susceptibility to, 13} phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypogonadotropic hypogonadism 16 with or without anosmia} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypogonadotropic hypogonadism 16 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 7, with or without av conduction defects Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.
bifid nose with or without anorectal and renal anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the bifid nose with or without anorectal and renal anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
androgen insensitivity, partial, with or without breast cancer Gene Set From OMIM Gene-Disease Associations genes associated with the androgen insensitivity, partial, with or without breast cancer phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 17 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, focal, with speech disorder and with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, progressive, with or without lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 2 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
woolly hair, autosomal recessive 2 with or without hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
ifap syndrome with or without bresheck syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set From OMIM Gene-Disease Associations genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency 16, with or without neurologic abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency 16, with or without neurologic abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 5 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine with or without aura, susceptibility to Gene Set From OMIM Gene-Disease Associations genes associated with the migraine with or without aura, susceptibility to phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 3, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 3, with or without situs inversus 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.
acrodysostosis 2, with or without hormone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the acrodysostosis 2, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperproinsulinemia, familial, with or without diabetes Gene Set From OMIM Gene-Disease Associations genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset.
left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 7 without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 7 without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
anterior segment anomalies with or without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.
sweat chloride elevation without cf Gene Set From OMIM Gene-Disease Associations genes associated with the sweat chloride elevation without cf phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.
?cardiac conduction disease with or without dilated cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 10, with or without ftd Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 10, with or without ftd phenotype from the curated OMIM Gene-Disease Associations dataset.
goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set From OMIM Gene-Disease Associations genes associated with the goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated OMIM Gene-Disease Associations dataset.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET 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.
Nonmedullary Thyroid Carcinoma, With Or Without Cell Oxyphilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonmedullary Thyroid Carcinoma, With Or Without Cell Oxyphilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Respiratory Failure Without Hypercapnia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Respiratory Failure Without Hypercapnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyposis Of Gastric Fundus Without Polyposis Coli Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyposis Of Gastric Fundus Without Polyposis Coli in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Esophageal Atresia With Or Without Tracheoesophageal Fistula Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Atresia With Or Without Tracheoesophageal Fistula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
2P21 Microdeletion Syndrome Without Cystinuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 2P21 Microdeletion Syndrome Without Cystinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chagas' Disease Without Mention Of Organ Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chagas' Disease Without Mention Of Organ Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dengue Without Warning Signs Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dengue Without Warning Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Acute Myeloid Leukemia Without Maturation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Acute Myeloid Leukemia Without Maturation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sweat Chloride Elevation Without Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sweat Chloride Elevation Without Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cholecystitis Without Calculus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cholecystitis Without Calculus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Segment Anomalies With Or Without Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Segment Anomalies With Or Without Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vacterl Association, X-Linked, With Or Without Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vacterl Association, X-Linked, With Or Without Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Panic Disorder Without Agoraphobia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Panic Disorder Without Agoraphobia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bpes Without Ovarian Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bpes Without Ovarian Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Malnutrition Without Mention Of Light-For-Dates Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Malnutrition Without Mention Of Light-For-Dates in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, X-Linked, With Or Without Neutropenia And/Or Platelet Abnormalities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, X-Linked, With Or Without Neutropenia And/Or Platelet Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Testicular Anomalies With Or Without Congenital Heart Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Testicular Anomalies With Or Without Congenital Heart Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Narcolepsy Without Cataplexy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Narcolepsy Without Cataplexy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia With Or Without Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia With Or Without Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia Without Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia Without Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypothyroidism Without Goiter Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypothyroidism Without Goiter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duane Retraction Syndrome 3 With Or Without Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duane Retraction Syndrome 3 With Or Without Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Malformations With Or Without Urinary Tract Defects Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Malformations With Or Without Urinary Tract Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Capillary Malformation Without Arteriovenous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Capillary Malformation Without Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cognitive Impairment With Or Without Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cognitive Impairment With Or Without Cerebellar Ataxia 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.
Genetic Hyperferritinemia Without Iron Overload Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genetic Hyperferritinemia Without Iron Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2023 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2023 dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2025 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2025 dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease short-rib thoracic dysplasia 9 with or without polydactyly from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 22 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 22 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 6 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 6 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 9 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 12 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 12 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Migraine without aura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Migraine without aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary autosomal recessive microcephaly 2 with or without cortical malformations Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary autosomal recessive microcephaly 2 with or without cortical malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 15 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 15 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 6 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 6 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acute myeloid leukemia without maturation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute myeloid leukemia without maturation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 4 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 4 with or without anosmia 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.
Developmental delay and seizures with or without movement abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay and seizures with or without movement abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 10 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 23 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 23 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 2 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 2 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 14 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 14 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial progressive hyperpigmentation with or without hypopigmentation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial progressive hyperpigmentation with or without hypopigmentation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 18 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 18 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 3 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 3 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 5 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 5 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 7 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 7 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 8 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 8 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 11 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 13 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 13 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 7 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 7 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 16 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 16 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 24 without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 24 without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Antley-Bixler syndrome without disordered steroidogenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Antley-Bixler syndrome without disordered steroidogenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Restless legs syndrome in migraine without aura Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Restless legs syndrome in migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Migraine without aura Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Migraine without aura 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.
Acute anterior uveitis (with or without ankylosing spondylitis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute anterior uveitis (with or without ankylosing spondylitis) 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.
Pulmonary arterial hypertension (without BMPR2 mutations) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary arterial hypertension (without BMPR2 mutations) 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.
Bicuspid aortic valve without aortic dilation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve without aortic dilation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sarcoidosis (non-Lofgren's syndrome without extrapulmonary manifestations) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sarcoidosis (non-Lofgren's syndrome without extrapulmonary manifestations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Spontaneous preterm birth without premature rupture of membranes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spontaneous preterm birth without premature rupture of membranes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Dentinogenesis Imperfecta Without Osteogenesis Imperfecta Gene Set

Dentinogenesis imperfecta - Shield's type II Gene Set

Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 Gene Set

Dentinogenesis Imperfecta Gene Set

Dentinogenesis imperfecta, shields type 3 Gene Set

dentinogenesis imperfecta Gene Set

dentinogenesis imperfecta Gene Set

dentinogenesis imperfecta Gene Set

dentinogenesis imperfecta, shields type ii Gene Set

dentinogenesis imperfecta, shields type iii Gene Set

Dentinogenesis Imperfecta - Shield'S Type Iii (Disorder) Gene Set

Dentinogenesis Imperfecta Gene Set

Dentinogenesis Imperfecta Limited To Primary Teeth Gene Set

Dentinogenesis imperfecta Gene Set

Dentinogenesis imperfecta Gene Set

Dentinogenesis imperfecta Gene Set

Osteogenesis imperfecta type 15 Gene Set

Osteogenesis imperfecta type 12 Gene Set

Osteogenesis imperfecta type 10 Gene Set

Osteogenesis imperfecta type 11 Gene Set

Osteogenesis imperfecta with normal sclerae, dominant form Gene Set

Osteogenesis imperfecta, recessive perinatal lethal Gene Set

Osteogenesis imperfecta Gene Set

Osteogenesis imperfecta type 5 Gene Set

Osteogenesis imperfecta type 13 Gene Set

Osteogenesis imperfecta Levin type Gene Set

OSTEOGENESIS IMPERFECTA, TYPE IIC Gene Set

Osteogenesis imperfecta type 2, thin-bone Gene Set

Osteogenesis imperfecta type I Gene Set

Osteogenesis imperfecta type 7 Gene Set

Osteogenesis imperfecta type 8 Gene Set

Osteogenesis imperfecta type III Gene Set

Osteogenesis imperfecta, type 2A Gene Set

Osteogenesis Imperfecta Gene Set

Osteogenesis imperfecta, type 7 Gene Set

Osteogenesis imperfecta, type 3 Gene Set

Osteogenesis Imperfecta, Type IX Gene Set

Osteogenesis imperfecta, type 4 Gene Set

Osteogenesis imperfecta, type VIII Gene Set

osteogenesis imperfecta Gene Set

osteogenesis imperfecta Gene Set

hearing loss/deafness; osteogenesis imperfecta Gene Set

mild osteogenesis imperfecta Gene Set

osteogenesis imperfecta Gene Set

Osteogenesis Imperfecta Gene Set

osteogenesis imperfecta, type vi Gene Set

osteogenesis imperfecta, type viii Gene Set

osteogenesis imperfecta, type vii Gene Set

osteogenesis imperfecta, type xi Gene Set

osteogenesis imperfecta, type xv Gene Set

osteogenesis imperfecta, type xiii Gene Set

osteogenesis imperfecta, type v Gene Set

osteogenesis imperfecta, type i Gene Set

osteogenesis imperfecta, type xiv Gene Set

osteogenesis imperfecta, type xii Gene Set

osteogenesis imperfecta, type ii Gene Set

osteogenesis imperfecta, type iv Gene Set

osteogenesis imperfecta, type ix Gene Set

osteogenesis imperfecta, type iii Gene Set

osteogenesis imperfecta, type x Gene Set

Osteogenesis Imperfecta Gene Set

Osteogenesis Imperfecta Gene Set

Type I collagen synthesis in the context of osteogenesis imperfecta Gene Set

Osteogenesis imperfecta Gene Set

Osteogenesis imperfecta type 19 Gene Set

Osteogenesis imperfecta Gene Set

Osteogenesis imperfecta type 20 Gene Set

Osteogenesis imperfecta type 5 Gene Set

Osteogenesis imperfecta type 1 Gene Set

Osteogenesis imperfecta type 4 Gene Set

Osteogenesis imperfecta type 8 Gene Set

Osteogenesis imperfecta type 7 Gene Set

Osteogenesis imperfecta type 12 Gene Set

Osteogenesis imperfecta type 11 Gene Set

Osteogenesis imperfecta type 14 Gene Set

Osteogenesis imperfecta type 6 Gene Set

Osteogenesis imperfecta type 2 Gene Set

Osteogenesis imperfecta type 9 Gene Set

Osteogenesis imperfecta type 10 Gene Set