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81873006: Iodide peroxidase defect (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
135820018 Iodide peroxidase defect en Synonym Active Entire term case insensitive SNOMED CT core module
135821019 Defective iodide peroxidase activity en Synonym Active Entire term case insensitive SNOMED CT core module
823192018 Iodide peroxidase defect (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
Iodide peroxidase defect Is a Inherited disorder of thyroid metabolism true Inferred relationship Existential restriction modifier
Iodide peroxidase defect Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Iodide peroxidase defect Finding site Thyroid structure false Inferred relationship Existential restriction modifier
Iodide peroxidase defect Occurrence Congenital false Inferred relationship Existential restriction modifier
Iodide peroxidase defect Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Iodide peroxidase defect 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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