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12427005: Congenital primary adrenocortical hypofunction (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
21388016 Congenital primary adrenocortical hypofunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
21389012 Congenital Addison disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
727839011 Congenital primary adrenocortical hypofunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
21388016 Congenital primary adrenocortical hypofunction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
21388016 Congenital primary adrenocortical hypofunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
21389012 Congenital Addison disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
727839011 Congenital primary adrenocortical hypofunction (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
727839011 Congenital primary adrenocortical hypofunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
66951000077117 insuffisance corticosurrénale primaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
66951000077117 insuffisance corticosurrénale primaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital primary adrenocortical hypofunction (disorder) Is a Adrenal cortical hypofunction false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Is a Congenital anomaly of adrenal gland false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Is a Adrenal cortical hypofunction (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital primary adrenocortical hypofunction (disorder) Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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