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


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

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 SNOMED CT core module
4593931017 Congenital iodine deficiency syndrome of neurological type en Synonym Active Entire term case insensitive SNOMED CT core module
4594735012 Endemic cretinism of neurological type en Synonym Active Entire term case insensitive SNOMED CT core 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
Congenital iodine deficiency syndrome of neurological type Causative agent Environmental agent false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Causative agent Iodine false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Finding site Thyroid structure false Inferred relationship Existential restriction modifier 2
Congenital iodine deficiency syndrome of neurological type Associated etiologic finding Iodine deficiency false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Due to Iodine deficiency false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of neurological type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of neurological type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of neurological type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of neurological type Finding site Thyroid structure true Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of neurological type Is a Neurological finding true Inferred relationship Existential restriction modifier

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

This concept is not in any reference sets

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