hypotrichosis 8
hypotrichosis has material basis in a autosomal recessive mutation of LPAR6 on chromosome 13q14.2
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hypotrichosis 8
Summary
hypotrichosis 8 is a rare disease[1].
Key Facts
- hypotrichosis 8's instance of is recorded as rare disease[2].
- hypotrichosis 8's instance of is recorded as class of disease[3].
- hypotrichosis 8's subclass of is recorded as hypotrichosis[4].
- hypotrichosis 8's subclass of is recorded as genetic disease[5].
- hypotrichosis 8's subclass of is recorded as autosomal recessive disease[6].
- hypotrichosis 8's subclass of is recorded as Woolly hair autosomal recessive[7].
- hypotrichosis 8's MeSH descriptor ID is recorded as C566950[8].
- hypotrichosis 8's OMIM ID is recorded as 278150[9].
- hypotrichosis 8's Disease Ontology ID is recorded as DOID:0110705[10].
- hypotrichosis 8's genetic association is recorded as LPAR6[11].
- hypotrichosis 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110705[12].
- hypotrichosis 8's exact match is recorded as http://identifiers.org/doid/DOID:0110705[13].
- hypotrichosis 8's UMLS CUI is recorded as C3279470[14].
- hypotrichosis 8's UMLS CUI is recorded as C1848435[15].
- hypotrichosis 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- hypotrichosis 8's Mondo ID is recorded as MONDO_0010206[17].
- hypotrichosis 8's UniProt disease ID is recorded as DI-01913[18].