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83664006: Idiopathic atrophic hypothyroidism (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
138752014 Idiopathic atrophic hypothyroidism en Synonym Active Case insensitive SNOMED CT core
138753016 Atrophic thyroiditis en Synonym Active Case insensitive SNOMED CT core
138754010 Idiopathic atrophic myxedema en Synonym Active Case insensitive SNOMED CT core
138755011 Gull disease en Synonym Active Case insensitive SNOMED CT core
505712017 Idiopathic atrophic myxoedema en Synonym Active Case insensitive SNOMED CT core
825345011 Idiopathic atrophic hypothyroidism (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
Idiopathic atrophic hypothyroidism Is a Idiopathic disease true Inferred relationship Some
Idiopathic atrophic hypothyroidism Is a Acquired atrophy of thyroid true Inferred relationship Some
Idiopathic atrophic hypothyroidism Associated morphology Atrophy true Inferred relationship Some 1
Idiopathic atrophic hypothyroidism Is a Degenerative disorder false Inferred relationship Some
Idiopathic atrophic hypothyroidism Is a Acquired hypothyroidism true Inferred relationship Some
Idiopathic atrophic hypothyroidism Associated morphology Atrophy false Inferred relationship Some 2
Idiopathic atrophic hypothyroidism Finding site Entire endocrine gonad false Inferred relationship Some
Idiopathic atrophic hypothyroidism Finding site Thyroid structure false Inferred relationship Some
Idiopathic atrophic hypothyroidism Occurrence Period of life between birth and death true Inferred relationship Some 1
Idiopathic atrophic hypothyroidism Finding site Thyroid structure true Inferred relationship Some 1

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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