Bilirubin encephalopathy

rare

Identifiers: MONDO:0018477 Orphanet:415286
Part of: Brain disorder Hereditary neurological disease Inborn disorder of bilirubin metabolism
Also known as: hyperbilirubinemic encephalopathy · kernicterus

Subtypes

Disease	ID	Subtypes
Kernicterus due to isoimmunization	MONDO:0006567

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