Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
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Urethral Diseases (D014522)
Parent Node:
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Urologic Neoplasms (D014571)
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Urethral Neoplasms (D014523)

       Child Nodes:



 Sister Nodes: 
..expandKidney Neoplasms (D007680) Child23
..expandUreteral Neoplasms (D014516)
..expandUrethral Neoplasms (D014523)
..expandUrinary Bladder Neoplasms (D001749) Child2
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:11403
Name:Urethral Neoplasms
Definition:Cancer or tumors of the URETHRA. Benign epithelial tumors of the urethra usually consist of squamous and transitional cells. Primary urethral carcinomas are rare and typically of squamous cells. Urethral carcinoma is the only urological malignancy that is more common in females than in males.
Alternative IDs:
ParentIDs:MESH:D014522|MESH:D014571
TreeNumbers:C04.588.945.947.945 |C12.758.820.937 |C12.777.767.601 |C13.351.937.820.890 |C13.351.968.767.601
Synonyms:Cancer of the Urethra |Cancer of Urethra |Cancers, Urethra |Cancers, Urethral |Cancer, Urethra |Cancer, Urethral |Neoplasms, Urethra |Neoplasms, Urethral |Neoplasm, Urethra |Neoplasm, Urethral |Urethra Cancer |Urethra Cancers |Urethral Cancer |Urethral Cancers |Urethr
Slim Mappings:Cancer|Urogenital disease (female)|Urogenital disease (male)
Reference: MedGen: D014523
MeSH: D014523
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants