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Summary Literature (0)
MIM:300123 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, WITH PANHYPOPITUITARISM

Xenbase Genes: sox3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000050 - isolated congenital growth hormone deficiency
MONDO:0010252 - 1st arch mandibular mesenchyme from neural crest
MONDO:0010615 - isolated growth hormone deficiency type III
MONDO:0019032 - X-linked intellectual disability with isolated growth hormone deficiency