NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD

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Summary

Literature (1)

MIM:614254 - NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD

Xenbase Genes: grin1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013655 - neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant
MONDO:0100172 - intellectual disability, autosomal dominant

MONDO:0013655 - neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

MONDO:0100172 - intellectual disability, autosomal dominant

Disease Ontology (DO):

DOID:0070038 - autosomal dominant intellectual developmental disorder 8

DOID:0070038 - autosomal dominant intellectual developmental disorder 8