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1197359006: Familial colorectal cancer type X (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4695998013 Familial colorectal cancer type X (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4695999017 Familial colorectal cancer type X en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4696000015 FCCTX - familial colorectal cancer type X en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399724019 A rare inherited cancer-predisposing syndrome characterized by the fulfilment of the Amsterdam criteria for hereditary nonpolyposis colorectal cancer (HNPCC) but without alterations, either somatic or germline, in the DNA mismatch repair (MMR) genes. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399725018 A rare inherited cancer-predisposing syndrome characterised by the fulfilment of the Amsterdam criteria for hereditary nonpolyposis colorectal cancer (HNPCC) but without alterations, either somatic or germline, in the DNA mismatch repair (MMR) genes. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4695998013 Familial colorectal cancer type X (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4695999017 Familial colorectal cancer type X en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4696000015 FCCTX - familial colorectal cancer type X en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4695996012 A rare hereditary nonpolyposis colon cancer defined in individuals meeting the Amsterdam criteria for Lynch syndrome, but lacking germline mutations in the mismatch repair genes. It is characterised by a later onset, preferential involvement of distal colon and rectum, lower risk of developing extracolonic cancer, a higher adenoma/carcinoma ratio, a higher differentiation of tumour cells, a more heterogeneous tumour architecture and an infiltrative growth pattern when compared to Lynch syndrome cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4695997015 A rare hereditary nonpolyposis colon cancer defined in individuals meeting the Amsterdam criteria for Lynch syndrome, but lacking germline mutations in the mismatch repair genes. It is characterized by a later onset, preferential involvement of distal colon and rectum, lower risk of developing extracolonic cancer, a higher adenoma/carcinoma ratio, a higher differentiation of tumor cells, a more heterogeneous tumor architecture and an infiltrative growth pattern when compared to Lynch syndrome cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399724019 A rare inherited cancer-predisposing syndrome characterized by the fulfilment of the Amsterdam criteria for hereditary nonpolyposis colorectal cancer (HNPCC) but without alterations, either somatic or germline, in the DNA mismatch repair (MMR) genes. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399725018 A rare inherited cancer-predisposing syndrome characterised by the fulfilment of the Amsterdam criteria for hereditary nonpolyposis colorectal cancer (HNPCC) but without alterations, either somatic or germline, in the DNA mismatch repair (MMR) genes. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3452721001000110 Familiäres kolorektales Karzinom Typ X de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3452721001000110 Familiäres kolorektales Karzinom Typ X de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial colorectal cancer type X (disorder) Is a Hereditary nonpolyposis colon cancer (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial colorectal cancer type X (disorder) Finding site Colon structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial colorectal cancer type X (disorder) Associated morphology Malignant neoplasm, primary false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial colorectal cancer type X (disorder) Associated morphology Malignant neoplasm (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial colorectal cancer type X (disorder) Pathological process (attribute) Malignant proliferation of primary neoplasm (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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