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155571000146107: hereditair 'non-polyposis'-colorectaal carcinoom door MSH2-mutatie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
13071551000146116 Hereditary nonpolyposis colon cancer caused by MSH2 mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13071561000146118 Hereditary nonpolyposis colon cancer caused by MSH2 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13071571000146112 HNPCC by MSH2 mutation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13071581000146114 Lynch syndrome type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13092431000146113 hereditair 'non-polyposis'-coloncarcinoom door MSH2-mutatie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13092441000146117 hereditair 'non-polyposis'-colorectaal carcinoom door MSH2-mutatie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13092451000146119 hereditair 'non-polyposis'-colorectaal carcinoom door MSH2-mutatie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13092461000146116 HNPCC1 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13092471000146110 Lynch-syndroom 1 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13092481000146112 HNPCC door MSH2-mutatie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary nonpolyposis colon cancer caused by MSH2 mutation (disorder) Is a Lynch syndrome (disorder) true Inferred relationship Some
Hereditary nonpolyposis colon cancer caused by MSH2 mutation (disorder) Associated morphology primair maligne neoplasma (afwijkende morfologie) false Inferred relationship Some 1
Hereditary nonpolyposis colon cancer caused by MSH2 mutation (disorder) Is a HNPCC - hereditary nonpolyposis colon cancer true Inferred relationship Some
Hereditary nonpolyposis colon cancer caused by MSH2 mutation (disorder) Finding site Colon structure true Inferred relationship Some 1
Hereditary nonpolyposis colon cancer caused by MSH2 mutation (disorder) Associated morphology Malignant neoplasm (morphologic abnormality) true Inferred relationship Some 1
Hereditary nonpolyposis colon cancer caused by MSH2 mutation (disorder) Pathological process (attribute) Malignant proliferation of primary neoplasm (qualifier value) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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