Papillary renal cell carcinoma, familial

Preferred Label : Papillary renal cell carcinoma, familial;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0537944;

UMLS CUI

C2931899;

CISMeF manual mappings
- Hereditary papillary renal cell carcinoma [ORDO Disease]
Currated CISMeF NLP mapping
- Familial papillary renal cell carcinoma [ICD-11 More detail]
- Hereditary Papillary Renal Cell Carcinoma [NCIt concept]
- Hereditary papillary renal carcinoma [MedDRA Preferred Term]
- Hereditary papillary renal cell carcinoma (disorder) [SNOMED CT concept]
- familial renal papillary carcinoma [DO Concept]
Related record
- papillary renal cell carcinoma, sporadic [MeSH Supplementary Concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary papillary renal cell carcinoma [ORDO Disease]
Validated automatic mappings to BTNT
- Renal cell carcinoma, papillary, 1 [OMIM Phenotype]