Disease-gene associations mined from literature

Human genes for Leigh disease

Leigh disease [DOID:3652]

A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.

Synonyms:  Leigh disease,  DOID:3652,  Leigh disorder,  Leigh syndrome,  Infantile necrotizing encephalomyelopathy ...

Linkouts:  OMIM #1 #2 #3 #4