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systemic scleroderma

^ http://purl.obolibrary.org/obo/DOID_418


A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. [ sn:IEDB ]

Synonyms: PSS, systemic sclerosis, progressive systemic sclerosis, Scleroderma syndrome, Scleroderma

Term info

database cross reference
  • MESH:D012595
  • UMLS_CUI:C0036421
  • ICD10CM:M34.9
  • CSP2005:4008-0097
  • GARD:9748
  • EFO:0000717
  • MTHICD9_2006:710.1
  • sn:IEDB
  • NCI:C72070
  • SNOMEDCT_US_2018_03_01:89155008
  • ICD9CM:710.1
  • ICD9CM_2006:710.1
  • OMIM:181750
  • ICD10CM:M34.0
Subsets

NCIthesaurus

has obo namespace

disease_ontology

id

DOID:418

Term relations