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autosomal dominant Robinow syndrome
Disease Summary
Associated Targets (3)
Tbio
2
Tchem
1
Mondo Description Autosomal dominant Robinow syndrome (DRS) is the more common type of Robinow syndrome (RS) characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia.
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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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:3107
SCTID:76520005
UMLS:CN203673
MONDO:0008389
High level summary of knowledge for a disease, including descriptions and datasource references.