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DO Term : systemic scleroderma [DOID:418] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
MESH:D012595,
ICD10CM:M34.0,
NCI:C72070,
OMIM:181750,
Scleroderma,
UMLS_CUI:C0036421,
181750,
EFO:0000717,
systemic sclerosis,
Scleroderma syndrome,
GARD:9748,
SNOMEDCT_US_2023_03_01:89155008,
ICD9CM:710.1,
progressive systemic sclerosis

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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