Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | autosomal dominant intellectual developmental disorder 31 | | ISO | CDC25C (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY more ... | ClinVar | PMID:28492532 | familial adenomatous polyposis 1 | | ISO | CDC25C (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Familial adenomatous polyposis 1 | ClinVar | PMID:17963004 more ... | genetic disease | | ISO | CDC25C (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | Hereditary Neoplastic Syndromes | | ISO | CDC25C (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:17963004 more ... | Hereditary Neoplastic Syndromes | | ISO | CDC25C (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:18487285 more ... | Neurodevelopmental Disorders | | ISO | CDC25C (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Neurodevelopmental disorder | ClinVar | PMID:25741868 | STING-associated vasculopathy with onset in infancy | | ISO | CDC25C (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: STING-associated vasculopathy with onset in infancy | ClinVar | PMID:28492532 | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - CTD
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