hypotrichosis 2
hypotrichosis that has material basis in a autosomal dominant mutation of CDSN on chromosome 6p21.33
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hypotrichosis 2
Summary
hypotrichosis 2 is a rare disease[1].
Key Facts
- hypotrichosis 2's instance of is recorded as rare disease[2].
- hypotrichosis 2's instance of is recorded as class of disease[3].
- hypotrichosis 2's subclass of is recorded as hypotrichosis[4].
- hypotrichosis 2's subclass of is recorded as genetic disease[5].
- hypotrichosis 2's subclass of is recorded as autosomal dominant disease[6].
- hypotrichosis 2's OMIM ID is recorded as 146520[7].
- hypotrichosis 2's Disease Ontology ID is recorded as DOID:0110699[8].
- hypotrichosis 2's genetic association is recorded as CDSN[9].
- hypotrichosis 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110699[10].
- hypotrichosis 2's exact match is recorded as http://identifiers.org/doid/DOID:0110699[11].
- hypotrichosis 2's UMLS CUI is recorded as C1840299[12].
- hypotrichosis 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- hypotrichosis 2's Mondo ID is recorded as MONDO_0007805[14].
- hypotrichosis 2's risk factor is recorded as smoking[15].
- hypotrichosis 2's UniProt disease ID is recorded as DI-01802[16].