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 is a type of hypotrichosis[4].
- hypotrichosis 2 is a type of genetic disease[5].
- hypotrichosis 2 is a type of autosomal dominant disease[6].
- hypotrichosis 2's genetic association is recorded as CDSN[7].
- hypotrichosis 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110699[8].
- hypotrichosis 2's exact match is recorded as http://identifiers.org/doid/DOID:0110699[9].
- hypotrichosis 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
- hypotrichosis 2's risk factor is recorded as smoking[11].