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81873006: Iodide peroxidase defect (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
135820018 Iodide peroxidase defect en Synonym Active Case insensitive SNOMED CT core
135821019 Defective iodide peroxidase activity en Synonym Active Case insensitive SNOMED CT core
823192018 Iodide peroxidase defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Iodide peroxidase defect Occurrence Congenital false Inferred relationship Some
Iodide peroxidase defect Is a Inherited disorder of thyroid metabolism true Inferred relationship Some
Iodide peroxidase defect Occurrence Congenital true Inferred relationship Some 1
Iodide peroxidase defect Finding site Thyroid structure true Inferred relationship Some 1
Iodide peroxidase defect Finding site Entire endocrine gonad false Inferred relationship Some
Iodide peroxidase defect Finding site Thyroid structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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