Galloway-Mowat syndrome 3

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Summary

Literature (0)

DOID:0080245 - Galloway-Mowat syndrome 3

Disease Ontology Definition:A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11.

Synonyms:

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

: osgep

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0033007 - DNAH8

MONDO:0033007 - DNAH8

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

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

Parent(s): autosomal recessive disease (is_a), Galloway-Mowat syndrome (is_a)