63127008: Thyroglobulin synthesis defect (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect

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

\Finding of thyroid gland\Disorder of thyroid gland\...

\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goiter\Thyroglobulin synthesis defect

\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect

\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect

\Disorder of neck\Disorder of thyroid gland\...

\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goiter\Thyroglobulin synthesis defect

\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect

\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Disorder of neck\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Disorder of neck\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of neck\Disorder of thyroid gland\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Congenital disease\Congenital hypothyroidism\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Congenital disease\Inborn error of metabolism\Dyshormonogenic goiter\Thyroglobulin synthesis defect
\Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect

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

Descriptions:

Id Description Lang Type Status Case? Module

104935010 Thyroglobulin synthesis defect en Synonym Active Entire term case insensitive SNOMED CT core module

104936011 Hypothyroidism due to thyroglobulin biosynthetic defect en Synonym Active Entire term case insensitive SNOMED CT core module

104937019 Genetic defect in thyroid hormonogenesis V en Synonym Active Only initial character case insensitive SNOMED CT core module

499490011 Hypothyroidism due to thyroglobulin synthesis defect en Synonym Active Entire term case insensitive SNOMED CT core module

802376015 Thyroglobulin synthesis defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Thyroglobulin synthesis defect	Is a	Inherited disorder of thyroid metabolism	true	Inferred relationship	Existential restriction modifier
Thyroglobulin synthesis defect	Is a	Hypothyroidism	false	Inferred relationship	Existential restriction modifier
Thyroglobulin synthesis defect	Is a	Dyshormonogenic goiter	true	Inferred relationship	Existential restriction modifier
Thyroglobulin synthesis defect	Finding site	Entire endocrine gonad	false	Inferred relationship	Existential restriction modifier
Thyroglobulin synthesis defect	Finding site	Thyroid structure	false	Inferred relationship	Existential restriction modifier	1
Thyroglobulin synthesis defect	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Thyroglobulin synthesis defect	Associated morphology	Hyperplasia	false	Inferred relationship	Existential restriction modifier	1
Thyroglobulin synthesis defect	Associated morphology	Hyperplasia	false	Inferred relationship	Existential restriction modifier	1
Thyroglobulin synthesis defect	Finding site	Thyroid structure	false	Inferred relationship	Existential restriction modifier	1
Thyroglobulin synthesis defect	Associated morphology	Enlargement	false	Inferred relationship	Existential restriction modifier	2
Thyroglobulin synthesis defect	Finding site	Entire thyroid gland	false	Inferred relationship	Existential restriction modifier	2
Thyroglobulin synthesis defect	Is a	Congenital hypothyroidism	false	Inferred relationship	Existential restriction modifier
Thyroglobulin synthesis defect	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Thyroglobulin synthesis defect	Interprets	Thyroid hormone measurement	false	Inferred relationship	Existential restriction modifier	3
Thyroglobulin synthesis defect	Has interpretation	Above reference range	false	Inferred relationship	Existential restriction modifier	3
Thyroglobulin synthesis defect	Finding site	Entire thyroid gland	true	Inferred relationship	Existential restriction modifier	1
Thyroglobulin synthesis defect	Associated morphology	Enlargement	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
104935010	Thyroglobulin synthesis defect	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
104936011	Hypothyroidism due to thyroglobulin biosynthetic defect	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
104937019	Genetic defect in thyroid hormonogenesis V	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
499490011	Hypothyroidism due to thyroglobulin synthesis defect	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
802376015	Thyroglobulin synthesis defect (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module