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scleroderma
Disease Summary
Associated Targets (255)
Tbio
180
Tchem
36
Tdark
27
Tclin
12
Mondo Description 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).
Disease Ontology Description A rheumatic disease and collagen disease that involves the abnormal growth of connective tissue, which supports the skin and internal organs.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:419
NCIT:C26746
Orphanet:801
MONDO:0019340
High level summary of knowledge for a disease, including descriptions and datasource references.