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703233008: Familial hyperaldosteronism type 2 (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3007668015 Familial hyperaldosteronism type 2 en Synonym Active Case insensitive SNOMED CT core
3007801010 Familial hyperaldosteronism type 2 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3008068017 A genetic cause of hypertension secondary to primary aldosteronism that is not suppressed with dexamethasone. Patients present with an adrenal adenoma that secretes aldosterone. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hyperaldosteronism type 2 Is a Familial hyperaldosteronism true Inferred relationship Some
Familial hyperaldosteronism type 2 Finding site Adrenal cortex 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

Strength reference set

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