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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 Diseases (D014522)
..Starting node ..Urethral Obstruction (D014524)
Child Nodes:
........Cervical ribs sprengel anomaly anal atresia urethral obstruction (C538072)
........Kashani Strom Utley syndrome (C537010)
........Selig Benacerraf Greene syndrome (C535840)
........Urethral obstruction sequence (C536477)
........Urethral Stricture (D014525)
........Urinary Bladder Neck Obstruction (D001748)
Sister Nodes:
..Epispadias (D004842) 1
..Penoscrotal transposition (C536650)
..Urethral Neoplasms (D014523)
..Urethral Obstruction (D014524) 6
..Urethritis (D014526)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11404
Name:	Urethral Obstruction
Definition:	Partial or complete blockage in any part of the URETHRA that can lead to difficulty or inability to empty the URINARY BLADDER. It is characterized by an enlarged, often damaged, bladder with frequent urges to void.
Alternative IDs:
ParentIDs:	MESH:D014522
TreeNumbers:	C12.777.767.700 \|C13.351.968.767.700
Synonyms:	Obstructions, Urethral \|Obstruction, Urethral \|Urethral Obstructions
Slim Mappings:	Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D014524 MeSH: D014524 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants