hypotrichosis 13
hypotrichosis that has material basis in a autosomal dominant mutation of KRT71 on chromosome 12q13.13
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hypotrichosis 13
Summary
hypotrichosis 13 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- hypotrichosis 13's instance of is recorded as rare disease[3].
- hypotrichosis 13's instance of is recorded as class of disease[4].
- hypotrichosis 13 is a type of hypotrichosis[5].
- hypotrichosis 13 is a type of genetic disease[6].
- hypotrichosis 13 is a type of autosomal dominant disease[7].
- hypotrichosis 13's genetic association is recorded as KRT71[8].
- hypotrichosis 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110710[9].
- hypotrichosis 13's exact match is recorded as http://identifiers.org/doid/DOID:0110710[10].
- hypotrichosis 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
hypotrichosis 13 is known by 5 alternative names across languages and contexts.[2]