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1156815009: Familial adenomatous polyposis due to 5q22.2 microdeletion (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4576252015 Familial adenomatous polyposis due to 5q22.2 microdeletion (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4576253013 Familial adenomatous polyposis due to 5q22.2 microdeletion en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial adenomatous polyposis due to 5q22.2 microdeletion Due to 5q22.2 deletion syndrome true Inferred relationship Existential restriction modifier 2
Familial adenomatous polyposis due to 5q22.2 microdeletion Associated morphology Multiple polyps true Inferred relationship Existential restriction modifier 1
Familial adenomatous polyposis due to 5q22.2 microdeletion Is a Familial multiple polyposis syndrome true Inferred relationship Existential restriction modifier
Familial adenomatous polyposis due to 5q22.2 microdeletion Finding site Structure of large intestine true Inferred relationship Existential restriction modifier 1
Familial adenomatous polyposis due to 5q22.2 microdeletion Is a Gastrointestinal complication true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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