NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR

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Summary

Literature (0)

MIM:617820 - NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR

Xenbase Genes: grin1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0060629 - neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive

MONDO:0060629 - neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive