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radio-renal syndrome
Disease Summary
Associated Targets ()
Mondo Description Radio-renal syndrome is a rare developmental defect during embryogenesis characterized by variable upper limb reduction defects and renal anomalies. Patients typically present absence/hypoplasia of digits, radii and/or ulnae, short stature and mild external ear malformation, as well as kidney agenesis or ectopia. There have been no further descriptions in the literature since 1983.
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.
GARD:0000224
MESH:C536267
OMIM:179280
Orphanet:3015
SCTID:766765009
UMLS:C2931146
MONDO:0008359
High level summary of knowledge for a disease, including descriptions and datasource references.