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

Global Variome shared LOVD

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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	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	WARS2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-02-01 09:21:38 +01:00 (CET)
Date last edited	N/A

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