43449002: Thyroglobulin proteolysis defect (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of head and neck region\Finding of neck region\...

\Finding of thyroid gland\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect

\Disorder of neck (disorder)\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect
\Disease\Disorder of neck (disorder)\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect
\Disease\Congenital disease (disorder)\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin proteolysis defect

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

4456951000172115 proteolysedefect van Tg nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4456961000172118 proteolysedefect van thyreoglobuline nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4456971000172110 thyroglobulineproteolysedefect nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

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