AICA-ribosiduria
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AICA-ribosiduria
Summary
AICA-ribosiduria is a developmental defect during embryogenesis[1]. AICA-ribosiduria is known by 6 alternative names across languages and contexts.[2]
Key Facts
- AICA-ribosiduria's instance of is recorded as developmental defect during embryogenesis[3].
- AICA-ribosiduria's instance of is recorded as rare disease[4].
- AICA-ribosiduria's instance of is recorded as class of disease[5].
- AICA-ribosiduria is a type of inborn disorder of purine metabolism[6].
- AICA-ribosiduria is a type of hereditary retinal dystrophy[7].
- AICA-ribosiduria is a type of developmental anomaly of metabolic origin[8].
- AICA-ribosiduria is a type of genetic macular dystrophy[9].
- AICA-ribosiduria is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[10].
- AICA-ribosiduria is a type of syndromic neurometabolic disease with non-X-linked intellectual disability[11].
- AICA-ribosiduria's genetic association is recorded as ATIC[12].
- AICA-ribosiduria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_250977[13].
Why It Matters
AICA-ribosiduria is known by 6 alternative names across languages and contexts.[2]