X-linked panhypopituitarism

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Summary

Literature (0)

DOID:0111779 - X-linked panhypopituitarism

Disease Ontology Definition:A combined pituitary hormone deficiency that has_material_basis_in duplications in the SOX3 gene on chromosome Xq27.1.

Synonyms: PHPX, pituitary dwarfism IV

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: sox3

MIM:

MIM:312000 - PANHYPOPITUITARISM, X-LINKED; PHPX

MIM:312000 - PANHYPOPITUITARISM, X-LINKED; PHPX

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): combined pituitary hormone deficiency (is_a), X-linked monogenic disease (is_a)