hypotrichosis, localized, autosomal recessive 1

Preferred Label : hypotrichosis, localized, autosomal recessive 1;

MeSH note : mutation in desmoglein-4;

MeSH synonym : hypotrichosis, localized, autosomal recessive;

Details

Origin ID

C564312;

UMLS CUI

C1842839;

Automatic exact mappings (from CISMeF team)
- Hypotrichosis 6 [OMIM Phenotype]
- hypotrichosis 6 [DO Concept]
MeSH term(s) associated for indexing
- hypotrichosis [MeSH Descriptor]
Record concept(s)
- hypotrichosis, localized, autosomal recessive 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypotrichosis 6 [OMIM Phenotype]
- hypotrichosis 6 [DO Concept]

Keyword's position in hierarchy(ies) :

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