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237565000: Congenital iodine deficiency syndrome of mixed type (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4593948013 Congenital iodine deficiency syndrome of mixed type (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4593949017 Congenital iodine deficiency syndrome of mixed type en Synonym Active Entire term case insensitive SNOMED CT core module
4594734011 Endemic cretinism of mixed type en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital iodine deficiency syndrome of mixed type Is a Endemic cretinism false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Finding site Thyroid structure false Inferred relationship Existential restriction modifier 2
Congenital iodine deficiency syndrome of mixed type Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Causative agent Iodine false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Causative agent Environmental agent false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Associated etiologic finding Iodine deficiency false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Due to Iodine deficiency false Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of mixed type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of mixed type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of mixed type Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of mixed type Finding site Thyroid structure true Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome of mixed type Is a Congenital iodine deficiency syndrome of neurological type true Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Is a Endemic congenital iodine deficiency syndrome of myxedematous type true Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Associated morphology Hard edema true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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