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43449002: Thyroglobulin proteolysis defect (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
72474015 Thyroglobulin proteolysis defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
780462013 Thyroglobulin proteolysis defect (disorder) en Fully specified name 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
Thyroglobulin proteolysis defect Is a Inherited disorder of thyroid metabolism true Inferred relationship Some
Thyroglobulin proteolysis defect Finding site Thyroid structure false Inferred relationship Some
Thyroglobulin proteolysis defect Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Thyroglobulin proteolysis defect Occurrence Congenital false Inferred relationship Some
Thyroglobulin proteolysis defect Occurrence Congenital true Inferred relationship Some 1
Thyroglobulin proteolysis defect Finding site Thyroid structure 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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