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Renal cell carcinoma

disorder

SNOMED 702391001CUI C0007134

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Renal carcinoma

HP:0005584

Related Conditions

Renal cell carcinoma of kidney except renal pelvis(child)

Tubulocystic renal cell carcinoma(child)

Papillary renal cell carcinoma(child)

Translocation renal cell carcinoma(child)

Acquired cystic disease associated renal cell carcinoma(child)

Familial renal cell carcinoma(child)

Mucinous tubular and spindle cell renal carcinoma(child)

Renal medullary carcinoma(child)

Chromophobe renal cell carcinoma(child)

Cystic renal cell carcinoma of kidney(child)

Clear cell carcinoma of kidney(child)

Primary hypernephroma(child)

Renal cell carcinoma of bilateral kidneys(child)

Adenocarcinoma(parent)

Malignant tumour of kidney(parent)

Quick Facts

SNOMED CT: 702391001
UMLS CUI: C0007134
Fully Specified Name: Renal cell carcinoma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 1
Known Treatments: 20

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.