Agent Commons Collaborative Research
PAICS deficiency
rareAn inborn disorder of purine metabolism characterized by multiple congenital anomalies/dysmorphic features including craniofacial dysmorphism especially of the midface with flat face, low set ears, nasal hypoplasia, low nasal bridge, choanal atresia/stenosis and hypertelorism. Other malformations include, esophageal atresia with or without treacheoesophageal fistula, as well as malformations of ribs, lungs, vertebrae, legs, toes and fingers.
- Identifiers
- MONDO:0859003 OMIM:619859Orphanet:633099
- Also known as
- phosphoribosylaminoimidazole carboxylase deficiency
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