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Grayu

Congenital Megabladder

Disease ID: disease_node_18268

Connections displayed (default: 10).

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Dbxref	MIM:618719
Subclassof	DOID_0050736, DOID_0080015, DOID_365
Data Source	DOID
Synonyms	MGBL
Doid Label	congenital megabladder
Doid Description	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.
Has Material Basis In	GENO_0000147
Disease Node Id	disease_node_18268
Doid Id	DOID_0112014
Disease Has Basis In	HP_0001197
Label	Congenital Megabladder

Outgoing r'ship SUBCLASS_OF to/from Physical Disorder(ID:disease_node_13159) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Urinary Bladder Diseases(ID:disease_node_1561) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)

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