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Gilbert syndrome

rare

An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.

Identifiers
MONDO:0007745 OMIM:143500Orphanet:357
Causal genes
UGT1A1
Part of
Hereditary hyperbilirubinemiaSyndromic disease
Also known as
familial cholemia · Gilbert disease · Gilbert's syndrome · hyperbilirubinemia type 1

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