hypotrichosis 3
hypotrichosis that has material basis in a autosomal dominant mutation of KRT74 on chromosome 12q13.13
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hypotrichosis 3
Summary
hypotrichosis 3 is a rare disease[1].
Key Facts
- hypotrichosis 3's instance of is recorded as rare disease[2].
- hypotrichosis 3's instance of is recorded as class of disease[3].
- hypotrichosis 3's subclass of is recorded as hypotrichosis[4].
- hypotrichosis 3's subclass of is recorded as genetic disease[5].
- hypotrichosis 3's subclass of is recorded as autosomal dominant disease[6].
- hypotrichosis 3's OMIM ID is recorded as 613981[7].
- hypotrichosis 3's Disease Ontology ID is recorded as DOID:0110700[8].
- hypotrichosis 3's genetic association is recorded as KRT74[9].
- hypotrichosis 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110700[10].
- hypotrichosis 3's exact match is recorded as http://identifiers.org/doid/DOID:0110700[11].
- hypotrichosis 3's UMLS CUI is recorded as C3151432[12].
- hypotrichosis 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- hypotrichosis 3's Mondo ID is recorded as MONDO_0013514[14].
- hypotrichosis 3's UniProt disease ID is recorded as DI-03172[15].