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1197359006: Familial colorectal cancer type X (disorder)


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

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 SNOMED CT core module
4695999017 Familial colorectal cancer type X en Synonym Active Only initial character case insensitive SNOMED CT core module
4696000015 FCCTX - familial colorectal cancer type X en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial colorectal cancer type X Is a Hereditary nonpolyposis colon cancer true Inferred relationship Existential restriction modifier
Familial colorectal cancer type X Finding site Colon structure true Inferred relationship Existential restriction modifier 1
Familial colorectal cancer type X Associated morphology Malignant neoplasm, primary false Inferred relationship Existential restriction modifier 1
Familial colorectal cancer type X Associated morphology Malignant neoplasm true Inferred relationship Existential restriction modifier 1
Familial colorectal cancer type X Pathological process Malignant proliferation of primary neoplasm true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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