Summary Literature (0)

MIM:616973 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 42; MRD42

Xenbase Genes: gnb1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014855 - FGF13

Disease Ontology (DO):

DOID:0070072 - autosomal dominant intellectual developmental disorder 42