Disease #05894 (NEMMLAS (neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with/without seizures (NEMMLAS)), OMIM:617710)

Official abbreviation NEMMLAS
Name neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with/without seizures (NEMMLAS)
OMIM ID 617710
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene WARS2
Associated tissues -
Disease features -
Remarks -