keratosis follicularis spinulosa decalvans, autosomal dominant

Preferred Label : keratosis follicularis spinulosa decalvans, autosomal dominant;

Origin ID

C567553;

UMLS CUI

C2748527;

Automatic exact mappings (from CISMeF team)
- autosomal dominant keratosis follicularis spinulosa decalvans [DO Concept]
Currated CISMeF NLP mapping
- Keratosis follicularis spinulosa decalvans, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- alopecia [MeSH Descriptor]
- darier disease [MeSH Descriptor]
- photophobia [MeSH Descriptor]
Record concept(s)
- keratosis follicularis spinulosa decalvans, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Keratosis follicularis spinulosa decalvans, autosomal dominant [OMIM Phenotype]