World Of Taxonomy
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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