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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 ..Urethritis (D014526)
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:	11407
Name:	Urethritis
Definition:	Inflammation involving the URETHRA. Similar to CYSTITIS, clinical symptoms range from vague discomfort to painful urination (DYSURIA), urethral discharge, or both.
Alternative IDs:
ParentIDs:	MESH:D014522
TreeNumbers:	C12.777.767.851 \|C13.351.968.767.851
Synonyms:	Urethritides
Slim Mappings:	Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D014526 MeSH: D014526 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants