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AICA-ribosiduria

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description AICA-ribosiduria is an extremely severe inborn error of purine biosynthesis characterized clinically in the single reported case to date by profound intellectual deficit, epilepsy, dysmorphic features of the knees, elbows, and shoulders and congenital blindness.
Uniprot Description A neurologically devastating inborn error of purine biosynthesis. Patients excrete massive amounts of AICA-riboside in the urine and accumulate AICA-ribotide and its derivatives in erythrocytes and fibroblasts. AICAR causes profound mental retardation, epilepsy, dysmorphic features and congenital blindness.
Mondo Term and Equivalent IDs
MONDO:0012099:  AICA-ribosiduria
MESH:C563876: 
Orphanet:250977: 
SCTID:725289009: 
UMLS:C1837530: 
UMLS:C4510943: