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Summary Literature (0)
DOID:0111272 - occipital horn syndrome


Disease Ontology Definition:A metal metabolism disorder characterized by hyperelastic and bruisable skin, hernias, bladder diverticula, hyperextensible joints, varicosities, abnormal copper transport, and multiple skeletal abnormalities that has_material_basis_in X-linked recessive inheritance of mutations in ATP7A on Xq21.1. This disorder is allelic to Menkes disease.

Synonyms: EDS IX, Ehlers-Danlos syndrome type 9, Ehlers-Danlos syndrome type IX, X-linked cutis laxa

Xenbase Genes : atp7a


OMIM:
OMIM:304150 - OCCIPITAL HORN SYNDROME; OHS

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): metal metabolism disorder (is_a)