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840509001: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3902186018 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3902187010 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3902186018 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3902187010 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5886841000241113 forme non classique d'hyperplasie surrénalienne congénitale due à un déficit en 21-hydroxylase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5886851000241111 forme non classique d'hyperplasie congénitale des glandes surrénales due à un déficit en 21-hydroxylase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5886841000241113 forme non classique d'hyperplasie surrénalienne congénitale due à un déficit en 21-hydroxylase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5886851000241111 forme non classique d'hyperplasie congénitale des glandes surrénales due à un déficit en 21-hydroxylase 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 adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Is a Disease of adrenal cortex false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Is a Congenital anomaly of adrenal gland true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Is a Adrenocortical hyperplasia true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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