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Summary Literature (0)
MIM:617710 - NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS

Xenbase Genes: wars2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060578 - neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures