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Summary Literature (0)
DOID:0112014 - congenital megabladder

Disease Ontology Definition:A bladder disease characterized by a massively dilated urinary bladder with disruption of the smooth muscle in the wall of the bladder that has_material_basis_in heterozygous mutation in the MYOCD gene on chromosome 17p12.

Synonyms: MGBL

Xenbase Genes :


MIM:
MIM:618719 - MEGABLADDER, CONGENITAL; MGBL

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), bladder disease (is_a), physical disorder (is_a)