Disease-gene associations mined from literature

Human genes for infantile liver failure syndrome

Infantile liver failure syndrome [DOID:0080716]

A syndrome that is characterized by acute liver failure, that occurs in the first year of life, which manifests with failure to thrive, hypotonia, moderate global developmental delay, seizures, abnormal liver function tests, microcytic anemia and elevated serum lactate.

Synonyms:  infantile liver failure syndrome,  DOID:0080716,  infantile liver failure disease,  infantile liver failure disorder,  infantile liver failure syndromes