Hereditary Kidney Wilms Tumor

Preferred Label : Hereditary Kidney Wilms Tumor;

NCIt synonyms : Hereditary Kidney Adenosarcoma; Hereditary Renal Adenosarcoma; Familial Kidney Wilms Tumor; Hereditary Kidney Nephroblastoma;

NCIt related terms : Hereditary Wilms Tumor;

NCIt definition : Familial embryonal neoplasm derived from nephrogenic blastemal cells. Several lines of differentiation, including blastemal, stromal and epithelial, are usually expressed. Comprises approximately 1% of Wilms tumors. (AFIP fascicle version 2.0);

Neoplastic status : Malignant;

Details

Origin ID

C8496;

UMLS CUI

C0677779;

Automatic exact mappings (from CISMeF team)
- hereditary Wilms' tumor [DO Concept]
DO Cross reference
- hereditary Wilms' tumor [DO Concept]
Disease excludes abnormal cell
- Neoplastic Glial Cell [NCIt concept]
Disease excludes normal cell origin
- Glial Cell [NCIt concept]
Disease may have findings
- Abdominal Mass [NCIt concept]
- Abdominal Pain [NCIt concept]
- Hematuria [NCIt concept]
- Hypertension [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)
- hereditary Wilms' tumor [DO Concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_excludes_molecular_abnormality
- DICER1 Gene Mutation [NCIt concept]
disease_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Blastemal Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Hereditary Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mixed Cellular Population [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
disease_has_molecular_abnormality
- Inactivating WT1 Gene Mutation [NCIt concept]
disease_has_normal_cell_origin
- Blastemal Cell [NCIt concept]
- Cell [NCIt concept]
- Embryonic Cell [NCIt concept]
- Nephrogenic Blastemal Cell [NCIt concept]
disease_has_normal_tissue_origin
- Embryonic Tissue [NCIt concept]
- Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Kidney [NCIt concept]
disease_mapped_to_chromosome
- Human Chromosome 11 [NCIt concept]
disease_mapped_to_gene
- WT1 Gene [NCIt concept]
related_to_genetic_biomarker
- CTR9 Gene [NCIt concept]
- FBXW7 Gene [NCIt concept]
- KDM3B Gene [NCIt concept]
- NYNRIN Gene [NCIt concept]
- REST Gene [NCIt concept]
- TRIM28 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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