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698854006: Hyperandrogenism due to non-classic type of 21-hydroxylase deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2981439012 Hyperandrogenism due to non-classic type of 21-hydroxylase deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2981501018 Hyperandrogenism due to non-classic type of 21-hydroxylase deficiency en Synonym Active Case insensitive SNOMED CT core
2988867018 Hyperandrogenism due to non-classic 21-hydroxylase deficiency en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperandrogenism due to non-classic 21-hydroxylase deficiency Is a Gynaecological endocrinology disorder true Inferred relationship Some
Hyperandrogenism due to non-classic 21-hydroxylase deficiency Is a Enzymopathy true Inferred relationship Some
Hyperandrogenism due to non-classic 21-hydroxylase deficiency Finding site Gonadal endocrine 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

Description inactivation indicator reference set

REFERS TO concept association reference set

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