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

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (1)

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

Xenbase Genes: grin1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013655 - intellectual disability, autosomal dominant 8
MONDO:0100172 - intellectual disability, autosomal dominant

MONDO:0013655 - intellectual disability, autosomal dominant 8

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