Trisomy 17 - CISMeF

Preferred Label : Trisomy 17;

NCIt definition : A chromosomal abnormality consisting of the presence of a third copy of chromosome 17 in somatic cells.;

Détails

Origin ID

C37865;

UMLS CUI

C5551620;

Automatic exact mappings (from CISMeF team)
- Chromosome 17 trisomy [MeSH concept]
- chromosome 17 trisomy [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Trisomy 17 [MedDRA Preferred Term]
See also inter- (CISMeF)
- Mosaic trisomy 17 syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome 17 trisomy [MeSH concept]
- Duplications of chromosome 17 [ICD-11 Subcategory]
- Mosaic trisomy 17 [ORDO Disease]
- Mosaic trisomy 17 syndrome (disorder) [SNOMED CT concept]
- Trisomy 17 [MedDRA Preferred Term]
- chromosome 17 trisomy [MeSH Supplementary Concept]
concept_is_in_subset
- ALL Authorized Value Terminology [NCIt concept]
- ALL Molecular Analysis Table [NCIt concept]
- CCPS Genetics Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Childhood Cancer Predisposition Study Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 17 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Advanced Papillary Renal Cell Carcinoma [NCIt concept]
- Hereditary Papillary Renal Cell Carcinoma [NCIt concept]
- Infantile Fibrosarcoma [NCIt concept]
- Locally Advanced Papillary Renal Cell Carcinoma [NCIt concept]
- Metastatic Papillary Renal Cell Carcinoma [NCIt concept]
- Papillary Renal Cell Carcinoma [NCIt concept]
- Renal Papillary Adenoma [NCIt concept]
- Sporadic Papillary Renal Cell Carcinoma [NCIt concept]
- Type 1 Papillary Renal Cell Carcinoma [NCIt concept]
- Type 2 Papillary Renal Cell Carcinoma [NCIt concept]
- Unresectable Papillary Renal Cell Carcinoma [NCIt concept]

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

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