ZFIN Human Disease: congenital megabladder

OBO ID: DOID:0112014

Term Name:	congenital megabladder		Search Ontology:
Synonyms:	MGBL
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. https://pubmed.ncbi.nlm.nih.gov/31513549/
References:	OMIM:618719
Ontology:	Human Disease ( DOID:0112014 )

Relationships

is a type of:	autosomal dominant disease bladder disease physical disorder autosomal dominant disease bladder disease physical disorder Show first 5 Terms

OTHER congenital megabladder PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYOCD	myocd	Megabladder, congenital	618719

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None