hypotrichosis 6
hypotrichosis that has material basis in a autosomal recessive mutation of DSG4 on chromosome 18q12.1
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hypotrichosis 6
Summary
hypotrichosis 6 is a rare disease[1].
Key Facts
- hypotrichosis 6's instance of is recorded as rare disease[2].
- hypotrichosis 6's instance of is recorded as class of disease[3].
- hypotrichosis 6's subclass of is recorded as hypotrichosis[4].
- hypotrichosis 6's subclass of is recorded as genetic disease[5].
- hypotrichosis 6's subclass of is recorded as autosomal recessive disease[6].
- hypotrichosis 6's MeSH descriptor ID is recorded as C564312[7].
- hypotrichosis 6's OMIM ID is recorded as 607903[8].
- hypotrichosis 6's OMIM ID is recorded as 607903[9].
- hypotrichosis 6's KEGG ID is recorded as H00784[10].
- hypotrichosis 6's Disease Ontology ID is recorded as DOID:0110703[11].
- hypotrichosis 6's genetic association is recorded as DSG4[12].
- hypotrichosis 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110703[13].
- hypotrichosis 6's exact match is recorded as http://identifiers.org/doid/DOID:0110703[14].
- hypotrichosis 6's UMLS CUI is recorded as C1842839[15].
- hypotrichosis 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- hypotrichosis 6's Mondo ID is recorded as MONDO_0011932[17].
- hypotrichosis 6's UniProt disease ID is recorded as DI-01912[18].