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


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

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 (core metadata concept) SNOMED CT core
4576253013 Familial adenomatous polyposis due to 5q22.2 microdeletion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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