63127008: Thyroglobulin synthesis defect (disorder)

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

\Viscus structure finding (finding)\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect (disorder)

\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Dyshormonogenic goiter\Thyroglobulin synthesis defect (disorder)
\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect (disorder)
\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect (disorder)
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Dyshormonogenic goiter\Thyroglobulin synthesis defect (disorder)
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect (disorder)
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Goiter\Dyshormonogenic goiter\Thyroglobulin synthesis defect (disorder)

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

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

Descriptions:

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
104935010	Thyroglobulin synthesis defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
104936011	Hypothyroidism due to thyroglobulin biosynthetic defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
104937019	Genetic defect in thyroid hormonogenesis V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499490011	Hypothyroidism due to thyroglobulin synthesis defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
802376015	Thyroglobulin synthesis defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
104935010	Thyroglobulin synthesis defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
104935010	Thyroglobulin synthesis defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
104936011	Hypothyroidism due to thyroglobulin biosynthetic defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
104936011	Hypothyroidism due to thyroglobulin biosynthetic defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
104937019	Genetic defect in thyroid hormonogenesis V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
104938012	GDTH V	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
499490011	Hypothyroidism due to thyroglobulin synthesis defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499490011	Hypothyroidism due to thyroglobulin synthesis defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
802376015	Thyroglobulin synthesis defect (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
802376015	Thyroglobulin synthesis defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
301461000077117	défaut de synthèse de la thyroglobuline	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
301461000077117	défaut de synthèse de la thyroglobuline	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module