JSON

Hypotrichosis simplex

^ http://www.orpha.net/ORDO/Orphanet_55654


Hypotrichosis simplex (HS) or hereditary hypotrichosis simplex (HHS) is characterized by reduced pilosity over the scalp and body (with sparse, thin, and short hair) in the absence of other anomalies.

Synonyms: Hereditary hypotrichosis simplex

Term info

database cross reference
  • ICD-10:L65.8 (Attributed)
  • OMIM:615059 (BTNT (broader term maps to a narrower term))
  • MeSH:C537160 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C1854310 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:615885 (BTNT (broader term maps to a narrower term))
  • ICD-10:L65.8 (NTBT (narrower term maps to a broader term))
  • OMIM:604379 (BTNT (broader term maps to a narrower term))
  • OMIM:614238 (BTNT (broader term maps to a narrower term))
  • OMIM:614237 (BTNT (broader term maps to a narrower term))
  • OMIM:278150 (BTNT (broader term maps to a narrower term))
  • OMIM:605389 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:618275 (BTNT (broader term maps to a narrower term))
  • OMIM:607903 (BTNT (broader term maps to a narrower term))
hasDbXref

OMIM:615059, OMIM:615885, OMIM:607903, OMIM:614238, OMIM:278150, OMIM:605389, OMIM:604379, OMIM:614237, UMLS:C1854310, OMIM:618275, MeSH:C537160, ICD-10:L65.8

notation

ORPHA:55654