23536000: Iodotyrosyl coupling defect (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Goitre\Dyshormonogenic goitre\Iodotyrosyl coupling defect

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

\Finding of thyroid gland\Thyroid disease\...

\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Iodotyrosyl coupling defect

\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect

\Goitre\Dyshormonogenic goitre\Iodotyrosyl coupling defect

\Disorder of neck\Thyroid disease\...

\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Iodotyrosyl coupling defect

\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect

\Goitre\Dyshormonogenic goitre\Iodotyrosyl coupling defect

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect
\Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect
\Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Goitre\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Disorder of neck\Thyroid disease\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Disorder of neck\Thyroid disease\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect
\Disease\Disorder of neck\Thyroid disease\Goitre\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect
\Disease\Congenital disease\Congenital hypothyroidism\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Congenital disease\Inborn error of metabolism\Dyshormonogenic goitre\Iodotyrosyl coupling defect
\Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Iodotyrosyl coupling defect

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1223110012 Hypothyroidism due to coupling defect en Synonym Active Case insensitive SNOMED CT core

39519010 Iodotyrosyl coupling defect en Synonym Active Case insensitive SNOMED CT core

39520016 Congenital thyroid hormone coupling defect en Synonym Active Case insensitive SNOMED CT core

39522012 Thyroid hormone coupling defect en Synonym Active Case insensitive SNOMED CT core

39523019 Genetic defect in thyroid hormonogenesis III en Synonym Active Initial character case insensitive SNOMED CT core

4590908018 GDTH III - genetic defect in thyroid hormonogenesis III en Synonym Active Case sensitive SNOMED CT core

753068012 Iodotyrosyl coupling defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1223110012	Hypothyroidism due to coupling defect	en	Synonym	Active	Case insensitive	SNOMED CT core
39519010	Iodotyrosyl coupling defect	en	Synonym	Active	Case insensitive	SNOMED CT core
39520016	Congenital thyroid hormone coupling defect	en	Synonym	Active	Case insensitive	SNOMED CT core
39522012	Thyroid hormone coupling defect	en	Synonym	Active	Case insensitive	SNOMED CT core
39523019	Genetic defect in thyroid hormonogenesis III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4590908018	GDTH III - genetic defect in thyroid hormonogenesis III	en	Synonym	Active	Case sensitive	SNOMED CT core
753068012	Iodotyrosyl coupling defect (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core