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CREST syndrome
Disease Summary
Associated Targets (19)
Tbio
11
Tdark
6
Tchem
2
Mondo Description CREST syndrome is a subtype of limited cutaneous systemic sclerosis (lcSSc) whose name is an acronym for the cardinal clinical features of the syndrome: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia.
Disease Ontology Description A syndrome characterized by calcinosis, Raynaud's phenomeno, esophageal dysmotility, sclerodactyly and telangiectasia.
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.
COHD:4135937
DOID:0060218
GARD:0012430
MESH:D017675
NCIT:C70646
Orphanet:90290
SCTID:31848007
UMLS:C0206138
MONDO:0019563
High level summary of knowledge for a disease, including descriptions and datasource references.