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237566004: Congenital iodine deficiency syndrome of neurological type (disorder)


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
4593930016 Congenital iodine deficiency syndrome of neurological type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4593931017 Congenital iodine deficiency syndrome of neurological type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4594735012 Endemic cretinism of neurological type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356024011 Congenital iodine deficiency syndrome - neurological type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356024011 Congenital iodine deficiency syndrome - neurological type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356025012 Endemic cretinism - neurological type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356025012 Endemic cretinism - neurological type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626314019 Congenital iodine deficiency syndrome - neurological type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
626314019 Congenital iodine deficiency syndrome - neurological type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4593930016 Congenital iodine deficiency syndrome of neurological type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4593931017 Congenital iodine deficiency syndrome of neurological type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4594735012 Endemic cretinism of neurological type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5018941000241118 syndrome congénital de carence en iode de type neurologique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5018941000241118 syndrome congénital de carence en iode de type neurologique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital iodine deficiency syndrome of neurological type Is a Endemic cretinism true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Causative agent (attribute) Environmental agent false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Causative agent (attribute) Iodine (substance) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Finding site Thyroid structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital iodine deficiency syndrome of neurological type Associated etiologic finding Iodine deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Due to Iodine deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital iodine deficiency syndrome of neurological type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital iodine deficiency syndrome of neurological type Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital iodine deficiency syndrome of neurological type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital iodine deficiency syndrome of neurological type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital iodine deficiency syndrome of neurological type Finding site Thyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital iodine deficiency syndrome of neurological type Is a Neurological finding true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital iodine deficiency syndrome of mixed type Is a True Congenital iodine deficiency syndrome of neurological type Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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