C201597Level 6
Osteootohepatoenteric Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** An exceedingly rare autosomal recessive condition caused by mutation (s) in the UNC45A gene, encoding protein unc-45 homolog A. It is characterized neonatal cholestasis, deafness, and bone fragility.
**Synonyms:** - O2HE - OOHE
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