DO_rare_slim has material basis in autosomal recessive disease transient infantile liver failure DOID:0080778 ORDO:217371 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. GARD:10593 disease_ontology MIM:613070 liver disease autosomal recessive inheritance