Gilbert syndrome

MONDO:0007745

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

Also known as: Gilbert disease, Gilbert syndrome, Gilbert's syndrome, familial cholemia, hyperbilirubinemia type 1, hyperbilirubinemia 1, hyperbilirubinemia, Arias type, hyperbilirubinemia, Gilbert type

0 clinical trials for this condition and its sub-types, 0 tagged with Gilbert syndrome itself.

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↑ Syndromic disease (7133) ↑ Hereditary hyperbilirubinemia (18)

Including sub-types (0) Tagged with Gilbert syndrome (0)

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