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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
838191000052117 medfött jodbristsyndrom, neurologisk typ sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital iodine deficiency syndrome of neurological type (disorder) Is a Endemic cretinism true Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Causative agent Environmental agent false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Associated morphology medfödd brist false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Occurrence Congenital false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Causative agent Iodine false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Finding site Thyroid structure false Inferred relationship Some 2
Congenital iodine deficiency syndrome of neurological type (disorder) Associated etiologic finding Iodine deficiency false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Associated morphology medfödd missbildning false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Due to Iodine deficiency false Inferred relationship Some
Congenital iodine deficiency syndrome of neurological type (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital iodine deficiency syndrome of neurological type (disorder) Associated morphology utvecklingsabnormitet false Inferred relationship Some 1
Congenital iodine deficiency syndrome of neurological type (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Congenital iodine deficiency syndrome of neurological type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital iodine deficiency syndrome of neurological type (disorder) Finding site Thyroid structure true Inferred relationship Some 1
Congenital iodine deficiency syndrome of neurological type (disorder) Is a Neurological finding true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital iodine deficiency syndrome of mixed type (disorder) Is a True Congenital iodine deficiency syndrome of neurological type (disorder) Inferred relationship Some

This concept is not in any reference sets

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