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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Urethral Obstruction (D014524)
Parent Node: Urinary Bladder Diseases (D001745)
..Starting node ..Urinary Bladder Neck Obstruction (D001748)
Child Nodes:
Sister Nodes:
..Bladder Exstrophy (D001746) 1
..Cystitis (D003556) 2
..Cystocele (D052858)
..Panic Disorder with Bladder Conditions (C566834)
..Pelvic lipomatosis (C535549)
..Urinary Bladder Calculi (D001744)
..Urinary Bladder Fistula (D001747) 1
..Urinary Bladder Neck Obstruction (D001748)
..Urinary Bladder Neoplasms (D001749) 2
..Urinary Bladder, Neurogenic (D001750)
..Urinary Bladder, Overactive (D053201)
..Vesico-Ureteral Reflux (D014718) 5
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11414
Name:	Urinary Bladder Neck Obstruction
Definition:	Blocked urine flow through the bladder neck, the narrow internal urethral opening at the base of the URINARY BLADDER. Narrowing or strictures of the URETHRA can be congenital or acquired. It is often observed in males with enlarged PROSTATE glands.
Alternative IDs:
ParentIDs:	MESH:D001745\|MESH:D014524
TreeNumbers:	C12.777.767.700.962 \|C12.777.829.760 \|C13.351.968.767.700.850 \|C13.351.968.829.601
Synonyms:	Bladder Neck Obstruction \|Bladder Outlet Obstruction
Slim Mappings:	Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D001748 MeSH: D001748 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants