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47757001: Corticosterone 18-monooxygenase deficiency (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
494915012 CMO II deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
494916013 Corticosterone methyl oxidase type II deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494917016 18-Hydroxycorticosterone dehydrogenase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
494918014 Aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
494919018 CAH - 18-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
785250014 Corticosterone 18-monooxygenase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
79583012 Corticosterone 18-monooxygenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
79584018 18-Hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
79585017 Aldosterone deficiency due to 18-hydroxylase defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
79586016 Corticosterone methyl oxidase type I deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
79587013 CMO I deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Corticosterone 18-monooxygenase deficiency (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) hyperplasie surrénale congénitale true Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Reproductive system hereditary disorder false Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Enzymopathy true Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Hereditary disorder of endocrine system (disorder) false Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Disorder of steroid metabolism true Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Aldosterone deficiency (disorder) true Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Inborn error of metabolism true Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) est un(e) (attribut) Congenital anomaly of adrenal gland false Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) morphologie associée (attribut) Hyperplasia (morphologic abnormality) true Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 2
Corticosterone 18-monooxygenase deficiency (disorder) localisation d'une constatation (attribut) cortex surrénalien true Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) morphologie associée (attribut) Congenital hyperplasia (morphologic abnormality) false Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) interprète (attribut) Nutritional deficiency state false Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) survenue (attribut) congénital false Inferred relationship Some
Corticosterone 18-monooxygenase deficiency (disorder) localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 1
Corticosterone 18-monooxygenase deficiency (disorder) localisation d'une constatation (attribut) Entire endocrine gonad (body structure) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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