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84781002: Sporadic cretinism (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
140556013 Sporadic cretinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
826697018 Sporadic cretinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5704941000172115 crétinisme sporadique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4236701000172115 sporadisch cretinisme nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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