transient infantile liver failure (DOID:0080778)
Alliance: disease page
Alt IDs: OMIM:613070, ORDO:217371
Definition: A liver disease that is characterized by elevated liver enzymes, jaundice, vomiting, coagulopathy, and hyperbilirubinemia, and the presence of increased serum lactate and that has_material_basis_in homozygous or compound heterozygous mutation in the TRMU gene, which is involved in mitochondrial protein translation, on chromosome 22q13.