Hereditary Kidney Oncocytoma

Preferred Label : Hereditary Kidney Oncocytoma;

NCIt synonyms : Familial Renal Oncocytoma; Hereditary Renal Oncocytoma;

NCIt definition : An inherited condition characterized by the development of kidney oncocytomas which are often bilateral and multifocal. This condition may be connected to Birt-Hogg-Dube syndrome.;

Neoplastic status : Undetermined;

Détails

Origin ID

C8960;

UMLS CUI

C0879606;

Automatic exact mappings (from CISMeF team)
- familial renal oncocytoma [DO Concept]
DO Cross reference
- familial renal oncocytoma [DO Concept]
Disease excludes abnormal cell
- Adenocarcinoma Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Malignant Connective and Soft Tissue Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Malignant Squamous Cell [NCIt concept]
- Malignant Transitional Cell [NCIt concept]
- Neoplastic Lymphocyte [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
- Neoplastic Squamous Cell [NCIt concept]
Disease excludes normal cell origin
- Endocrine-Stromal Cell [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]
UMLS correspondences (same concept)
- familial renal oncocytoma [DO Concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
disease_excludes_finding
- Borderline Lesion [NCIt concept]
- Lymphocytic Infiltrate [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mixed Neoplastic Glandular and Squamous Cell Population [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Glandular Cell [NCIt concept]
- Neoplastic Oncocyte [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Hereditary Lesion [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Genitourinary System [NCIt concept]
- Kidney [NCIt concept]
- Urinary System [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 1 [NCIt concept]
- Loss of Chromosome 14 [NCIt concept]
- t(5;11)(q35;q13) [NCIt concept]
disease_may_have_molecular_abnormality
- FLCN Gene Mutation [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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