Terminology Service for NFDI4Health
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scleroderma

Go to external page http://www.ebi.ac.uk/efo/EFO_1001993

Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc). [ ]

Term info

Label

scleroderma

Synonyms
  • Morphea "en coup de sabre"
  • dermatosclerosis
  • linear scleroderma
  • localized scleroderma
  • morphea
  • scleroderma
  • scleroderma (disease)
database cross reference
Subsets

disease_grouping, ordo_group_of_disorders

IAO 0000589

scleroderma (disease)

closeMatch

http://identifiers.org/meddra/10039710

exactMatch

http://purl.obolibrary.org/obo/DOID_419, http://purl.obolibrary.org/obo/NCIT_C26746, http://purl.obolibrary.org/obo/Orphanet_801

id

EFO:1001993

term editor

Gautier Koscielny