Renal pelvis squamous cell carcinoma
diseaseOn this page
Also known as epidermoid carcinoma of kidney pelvisepidermoid carcinoma of renal pelvisepidermoid carcinoma of the kidney pelvisepidermoid carcinoma of the renal pelviskidney pelvis epidermoid carcinomakidney pelvis squamous cell carcinomakidney renal pelvis squamous cell cancerrenal pelvis epidermoid carcinomarenal pelvis squamous cell cancersquamous cell carcinoma of kidney pelvissquamous cell carcinoma of renal pelvissquamous cell carcinoma of the kidney pelvissquamous cell carcinoma of the renal pelvis
Summary
Renal pelvis squamous cell carcinoma (MONDO:0003497) is a cancer. A subtype of squamous cell carcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | renal pelvis squamous cell carcinoma |
| Mondo ID | MONDO:0003497 |
| DOID | DOID:5534 |
| NCIT | C7732 |
| UMLS | C0238409 |
| MedGen | 66769 |
| Anatomy (UBERON) | UBERON:0001224 |
| Is cancer (heuristic) | yes |
Also known as: epidermoid carcinoma of kidney pelvis · epidermoid carcinoma of renal pelvis · epidermoid carcinoma of the kidney pelvis · epidermoid carcinoma of the renal pelvis · kidney pelvis epidermoid carcinoma · kidney pelvis squamous cell carcinoma · kidney renal pelvis squamous cell cancer · renal pelvis epidermoid carcinoma · renal pelvis squamous cell cancer · renal pelvis squamous cell carcinoma · squamous cell carcinoma of kidney pelvis · squamous cell carcinoma of renal pelvis · squamous cell carcinoma of the kidney pelvis · squamous cell carcinoma of the renal pelvis
Data availability: 1 cell line.
Disease family
This is a subtype of squamous cell carcinoma. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › epithelial neoplasm › squamous cell neoplasm › squamous cell carcinoma › renal pelvis squamous cell carcinoma
Related subtypes (38): bone squamous cell carcinoma, prostate squamous cell carcinoma, trachea squamous cell carcinoma, scrotum squamous cell carcinoma, skin squamous cell carcinoma, bladder squamous cell carcinoma, urethra squamous cell carcinoma, papillary squamous carcinoma, basaloid squamous cell carcinoma, pseudoglandular squamous cell carcinoma, thymus squamous cell carcinoma, ovarian squamous cell carcinoma, ureter squamous cell carcinoma, fallopian tube squamous cell carcinoma, squamous carcinoma in situ, keratinizing squamous cell carcinoma, squamous cell lung carcinoma, esophageal squamous cell carcinoma, squamous cell breast carcinoma, adenosquamous carcinoma, cervical squamous cell carcinoma, colorectal squamous cell carcinoma, endometrial squamous cell carcinoma, gallbladder squamous cell carcinoma, gastric squamous cell carcinoma, thyroid gland squamous cell carcinoma, vaginal squamous cell carcinoma, head and neck squamous cell carcinoma, squamous cell carcinoma of the corpus uteri, squamous cell carcinoma of penis, squamous cell carcinoma of the small intestine, squamous cell carcinoma of pancreas, squamous cell carcinoma of liver and intrahepatic biliary tract, human papillomavirus-related squamous cell carcinoma, sarcomatoid squamous cell carcinoma, vulvar squamous cell carcinoma, metastatic squamous cell carcinoma, pure squamous carcinoma of the urothelial tract
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.