About   Help   FAQ
Disease Ontology Browser
systemic scleroderma (DOID:418)
Alliance: disease page
Synonyms: progressive systemic sclerosis; PSS; Scleroderma; Scleroderma syndrome; systemic sclerosis
Alt IDs: OMIM:181750, EFO:0000717, ICD10CM:M34.0, ICD10CM:M34.9, ICD9CM_2006:710.1, ICD9CM:710.1, MESH:D012595, NCI:C72070, UMLS_CUI:C0036421
Definition: A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.

Disease References using Mouse Models (10)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
06/18/2019
MGI 6.14
The Jackson Laboratory