217710005: Congenital iodine deficiency syndrome (disorder)

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

\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Iodine deficiency syndrome\Congenital iodine deficiency syndrome
\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Finding of neck region\Disease of neck\Congenital anomaly of neck\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Iodine deficiency syndrome\Congenital iodine deficiency syndrome
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome due to non-infectious environmental agents\Congenital iodine deficiency syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of neck\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of endocrine gland\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of thyroid gland\Iodine deficiency syndrome\Congenital iodine deficiency syndrome
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of thyroid gland\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Congenital anomaly of endocrine gland\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Disease of neck\Congenital anomaly of neck\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Disease of neck\Disorder of thyroid gland\Iodine deficiency syndrome\Congenital iodine deficiency syndrome
\Disease\Disease of neck\Disorder of thyroid gland\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome due to non-infectious environmental agents\Congenital iodine deficiency syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of neck\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of endocrine gland\Congenital anomaly of the thyroid gland\Congenital iodine deficiency syndrome
\Disease\Nutritional disorder\Nutritional deficiency disorder (disorder)\Undernutrition\Deficiency of micronutrients\Mineral deficiency\Iodine deficiency\Iodine deficiency syndrome\Congenital iodine deficiency syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2010. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital iodine deficiency syndrome	Is a	Hypothyroidism	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Finding site	Thyroid structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital iodine deficiency syndrome	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Is a	Congenital anomaly of neck	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Is a	Multiple malformation syndrome due to non-infectious environmental agents	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Is a	Iodine deficiency syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Associated morphology	Congenital deficiency	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Associated etiologic finding	Iodine deficiency	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Due to	Iodine deficiency	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital iodine deficiency syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital iodine deficiency syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital iodine deficiency syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital iodine deficiency syndrome	Finding site	Thyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital iodine deficiency syndrome	Is a	Congenital anomaly of the thyroid gland	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital hypothyroidism without goitre	Is a	True	Congenital iodine deficiency syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)
Neurologic form of cretinism	Is a	False	Congenital iodine deficiency syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypothyroidism with diffuse goiter (disorder)	Is a	True	Congenital iodine deficiency syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)
Myxedematous form of cretinism (disorder)	Is a	True	Congenital iodine deficiency syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)
Endemic cretinism	Is a	True	Congenital iodine deficiency syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)
Sporadic cretinism	Is a	True	Congenital iodine deficiency syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
329964013	Congenital goitre	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329965014	Congenital iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329966010	Congenital goiter	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329968011	Cretinism	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329969015	Congenital hypothyroidism not due to iodine deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329971015	Fetal iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329972010	Infantile hypothyroidism	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
604105011	Congenital iodine deficiency syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2871641014	Foetal iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329964013	Congenital goitre	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329964013	Congenital goitre	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329965014	Congenital iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329965014	Congenital iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329966010	Congenital goiter	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329966010	Congenital goiter	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329967018	CHT - Congenital hypothyroidism	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
329968011	Cretinism	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329968011	Cretinism	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329969015	Congenital hypothyroidism not due to iodine deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329969015	Congenital hypothyroidism not due to iodine deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329970019	Endemic cretinism	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329971015	Fetal iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329971015	Fetal iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329972010	Infantile hypothyroidism	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329972010	Infantile hypothyroidism	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329973017	Congenital hypothyroidism	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
604105011	Congenital iodine deficiency syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
604105011	Congenital iodine deficiency syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2871641014	Foetal iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2871641014	Foetal iodine deficiency syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
911081000195112	sindrome da carenza di iodio congenita	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
425901000274114	Angeborenes Jodmangelsyndrom	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6921771000241117	syndrome de carence congénitale en iode	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6921771000241117	syndrome de carence congénitale en iode	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
911081000195112	sindrome da carenza di iodio congenita	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
425901000274114	Angeborenes Jodmangelsyndrom	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module