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84781002: Sporadic cretinism (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
140556013 Sporadic cretinism en Synonym Active Entire term case insensitive SNOMED CT core module
826697018 Sporadic cretinism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sporadic cretinism Is a Congenital hypothyroidism true Inferred relationship Existential restriction modifier
Sporadic cretinism Is a Multiple malformation syndrome due to non-infectious environmental agents false Inferred relationship Existential restriction modifier
Sporadic cretinism Is a Congenital iodine deficiency syndrome true Inferred relationship Existential restriction modifier
Sporadic cretinism Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Sporadic cretinism Occurrence Congenital false Inferred relationship Existential restriction modifier
Sporadic cretinism Causative agent Environmental agent false Inferred relationship Existential restriction modifier
Sporadic cretinism Finding site Thyroid structure false Inferred relationship Existential restriction modifier 2
Sporadic cretinism Associated etiologic finding Iodine deficiency false Inferred relationship Existential restriction modifier
Sporadic cretinism Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Sporadic cretinism Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Sporadic cretinism Due to Iodine deficiency false Inferred relationship Existential restriction modifier
Sporadic cretinism Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Sporadic cretinism Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Sporadic cretinism Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Sporadic cretinism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Sporadic cretinism Finding site Thyroid structure 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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