Chromophobe Renal Cell Carcinoma Associated with Birt-Hogg-Dube Syndrome

Preferred Label : Chromophobe Renal Cell Carcinoma Associated with Birt-Hogg-Dube Syndrome;

NCIt definition : Chromophobe renal cell carcinoma that develops in a patient with Birt-Hogg-Dube syndrome.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL562816;

Details

Origin ID

C155951;

UMLS CUI

C4744472;

Disease excludes abnormal cell
- Adenocarcinoma Clear Cell [NCIt concept]
- Malignant Squamous Cell [NCIt concept]
- Malignant Stromal Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
- Neoplastic Squamous Cell [NCIt concept]
Disease may have findings
- Flank Pain [NCIt concept]
- Hematuria [NCIt concept]
Has associated anatomic sites
- Genitourinary System [NCIt concept]
- Kidney [NCIt concept]
- Kidney and Ureter [NCIt concept]
- Urinary System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Mixed Neoplastic Glandular and Squamous Cell Population [NCIt concept]
disease_has_abnormal_cell
- Adenocarcinoma Cell [NCIt concept]
- Adenocarcinoma Cell with Abundant Cytoplasm [NCIt concept]
- Malignant Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Glandular Cell [NCIt concept]
disease_has_associated_disease
- Birt-Hogg-Dube Syndrome [NCIt concept]
disease_has_finding
- Carcinomatous Component Present [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_molecular_abnormality
- FLCN Gene Mutation [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
- Renal Tubular Epithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Renal Tubule Epithelium [NCIt concept]
disease_has_primary_anatomic_site
- Genitourinary System [NCIt concept]
- Kidney [NCIt concept]
- Renal Tubule [NCIt concept]
- Urinary System [NCIt concept]
disease_mapped_to_gene
- FLCN Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 1 [NCIt concept]
- Loss of Chromosome 10 [NCIt concept]
- Loss of Chromosome 13 [NCIt concept]
- Loss of Chromosome 17 [NCIt concept]
- Loss of Chromosome 2 [NCIt concept]
- Loss of Chromosome 21 [NCIt concept]
- Loss of Chromosome 6 [NCIt concept]
- Loss of Chromosome Y [NCIt concept]
pathogenesis_of_disease_involves_gene
- FLCN Gene [NCIt concept]
- FLCN wt Allele [NCIt concept]

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