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71578002: Steroid 21-monooxygenase deficiency, salt wasting type (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
118912012 Steroid 21-monooxygenase deficiency, salt wasting type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
118913019 Congenital adrenal hyperplasia, type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200220011 21-hydroxylase deficiency, salt wasting type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
811759010 Steroid 21-monooxygenase deficiency, salt wasting type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Steroid 21-monooxygenase deficiency, salt wasting type Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type survenue (attribut) congénital false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type est un(e) (attribut) Salt-losing congenital adrenal hyperplasia true Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type est un(e) (attribut) Deficiency of steroid 21-monooxygenase false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type morphologie associée (attribut) Hyperplasia (morphologic abnormality) true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type est un(e) (attribut) Congenital anomaly of adrenal gland false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type morphologie associée (attribut) Congenital hyperplasia (morphologic abnormality) false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, salt wasting type localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type survenue (attribut) congénital false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, salt wasting type morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 2
Steroid 21-monooxygenase deficiency, salt wasting type localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, salt wasting type survenue (attribut) congénital true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type localisation d'une constatation (attribut) cortex surrénalien true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type Due to 21-hydroxylase deficiency (disorder) false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type est un(e) (attribut) hyperplasie congénitale des surrénales par déficit en 21-hydroxylase classique true Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Some 2
Steroid 21-monooxygenase deficiency, salt wasting type localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type localisation d'une constatation (attribut) Entire endocrine gonad (body structure) false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type morphologie associée (attribut) Congenital hyperplasia (morphologic abnormality) false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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