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Summary Literature (0)
DOID:0081190 - autosomal recessive intellectual developmental disorder 18


Disease Ontology Definition:An autosomal recessive intellectual developmental disorder that is characterized by impaired intellectual development with or without epilepsy and that has_material_basis_in homozygous or compound heterozygous mutation in the MED23 gene on chromosome 6q23.

Synonyms:

Xenbase Genes : med23



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive intellectual developmental disorder (is_a)