Hereditary Colorectal Cancer Type X

Preferred Label : Hereditary Colorectal Cancer Type X;

NCIt synonyms : FCCTX; Familial Colorectal Cancer Type X;

NCIt definition : Hereditary nonpolyposis colorectal cancer syndrome characterized by the absence of germline mutations in DNA mismatch-repair genes.;

Details

Origin ID

C120084;

UMLS CUI

C3896578;

CISMeF manual mappings
- familial colorectal cancer type X [Disease (Nov.)]
Currated CISMeF NLP mapping
- Familial colorectal cancer Type X [ORDO Disease]
- Familial colorectal cancer type X (disorder) [SNOMED CT concept]
Has cytogenetic abnormalities
- Gain of Chromosome 20q [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Familial colorectal cancer type X (disorder) [SNOMED CT concept]
- familial colorectal cancer type X [Disease (Nov.)]
disease_excludes_molecular_abnormality
- Mismatch Repair Gene Inactivation [NCIt concept]
disease_has_associated_disease
- Colorectal Carcinoma [NCIt concept]
disease_has_finding
- Hereditary Lesion [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 18 [NCIt concept]

Keyword's position in hierarchy(ies) :

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