Disease #06817 (NDHMSR (Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive), OMIM:617820)

Official abbreviation	NDHMSR
Name	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive
OMIM ID	617820
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GRIN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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Global Variome shared LOVD