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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: Abnormalities, Multiple (D000015)
Parent Node: Urethral Diseases (D014522)
..Starting node ..Penoscrotal transposition (C536650)
Child Nodes:
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:	8776
Name:	Penoscrotal transposition
Definition:
Alternative IDs:
ParentIDs:	MESH:D000015\|MESH:D014522
TreeNumbers:	C12.777.767/C536650 \|C13.351.968.767/C536650 \|C16.131.077/C536650
Synonyms:	Congenital transposition of the penis \|Prepenile scrotum
Slim Mappings:	Congenital abnormality\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C536650 MeSH: C536650 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants