JSON

scleroderma

^ http://purl.obolibrary.org/obo/MONDO_0019340

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). [ Orphanet:801 ]

Term info

database cross reference
  • Orphanet:801 (MONDO:equivalentTo)
  • HP:0100324 (MONDO:otherHierarchy)
  • DOID:419 (MONDO:equivalentTo)
  • MedDRA:10039710 (Orphanet:801/e)
  • NCIT:C26746 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

IAO 0000589

scleroderma (disease)

closeMatch

http://identifiers.org/meddra/10039710

definition

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).

exactMatch

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

has exact synonym

scleroderma (disease), scleroderma, dermatosclerosis

id

MONDO:0019340

Term relations