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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: Constriction, Pathologic (D003251)
Parent Node: Hydronephrosis (D006869)
Parent Node: Oligohydramnios (D016104)
Parent Node: Peripheral Vascular Diseases (D016491)
Parent Node: Prune Belly Syndrome (D011535)
Parent Node: Urethral Obstruction (D014524)
..Starting node ..Urethral obstruction sequence (C536477)
Child Nodes:
Sister 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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11405
Name:	Urethral obstruction sequence
Definition:
Alternative IDs:
ParentIDs:	MESH:D003251\|MESH:D006869\|MESH:D011535\|MESH:D014524\|MESH:D016104\|MESH:D016491
TreeNumbers:	C12.777.419.307/C536477 \|C12.777.767.700/C536477 \|C13.351.968.419.307/C536477 \|C13.351.968.767.700/C536477 \|C13.703.560/C536477 \|C14.907.617/C536477 \|C16.131.077.745/C536477 \|C23.300.287/C536477
Synonyms:	Early urethral obstruction sequence
Slim Mappings:	Cardiovascular disease\|Congenital abnormality\|Pathology (anatomical condition)\|Pregnancy complication\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C536477 MeSH: C536477 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants