hypotrichosis simplex

Preferred Label : hypotrichosis simplex;

MeSH synonym : hereditary hypotrichosis simplex;

Origin ID

C537160;

UMLS CUI

C1854310;

Automatic exact mappings (from CISMeF team)
- Hereditary hypotrichosis simplex (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hypotrichosis simplex [ORDO Disease]
- hereditary hypotrichosis simplex [Disease (Nov.)]
MeSH term(s) associated for indexing
- hypotrichosis [MeSH Descriptor]
ORDO relation(s)
- Hypotrichosis simplex [ORDO Disease]
Record concept(s)
- Hypotrichosis simplex [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary hypotrichosis simplex (disorder) [SNOMED CT concept]
- Hypotrichosis 1 [OMIM Phenotype]
- Hypotrichosis simplex [ORDO Disease]
- hereditary hypotrichosis simplex [Disease (Nov.)]
- hypotrichosis 1 [DO Concept]