Human genes for transient infantile liver failure
Transient infantile liver failure [DOID:0080778]
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.
Synonyms: transient infantile liver failure, DOID:0080778, transient infantile liver failures