Disease-gene associations mined from literature

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