FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

52604008: Steroid 21-monooxygenase deficiency, simple virilizing type (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
1783827016 Steroid 21-hydroxylase deficiency, simple virilising type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1784215016 Steroid 21-hydroxylase deficiency, simple virilizing type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496368011 Steroid 21-monooxygenase deficiency, simple virilising type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496369015 Simple-virilising congenital adrenal hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496370019 Simple virilising adrenal hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496372010 Simple-virilizing congenital adrenal hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
790632010 Steroid 21-monooxygenase deficiency, simple virilizing type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
87546013 Steroid 21-monooxygenase deficiency, simple virilizing type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
87548014 Simple virilizing adrenal hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
87549018 Adrenogenital disorder due to 21-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
87550018 Congenital adrenal hyperplasia, type 1 en Synonym (core metadata concept) 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, simple virilising type Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, simple virilising type morphologie associée (attribut) Hyperplasia (morphologic abnormality) true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Congenital anomaly of trunk false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Congenital anomaly of adrenal gland false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Inborn error of metabolism false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Adrenal virilism false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Enzymopathy false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Hereditary disorder of endocrine system (disorder) false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) hyperplasie surrénale congénitale false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Reproductive system hereditary disorder false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Virilising syndrome of adrenal origin true Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) Disorder of steroid metabolism false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type morphologie associée (attribut) Congenital hyperplasia (morphologic abnormality) false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, simple virilising type localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, simple virilising type survenue (attribut) congénital false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, simple virilising type morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 2
Steroid 21-monooxygenase deficiency, simple virilising type localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, simple virilising type survenue (attribut) congénital true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, simple virilising type localisation d'une constatation (attribut) cortex surrénalien true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, simple virilising type Due to 21-hydroxylase deficiency (disorder) false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type est un(e) (attribut) hyperplasie congénitale des surrénales par déficit en 21-hydroxylase classique true Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Some 2
Steroid 21-monooxygenase deficiency, simple virilising type morphologie associée (attribut) Congenital hyperplasia (morphologic abnormality) false Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, simple virilising type localisation d'une constatation (attribut) Entire endocrine gonad (body structure) false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type survenue (attribut) congénital false Inferred relationship Some
Steroid 21-monooxygenase deficiency, simple virilising type localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Mild steroid 21-hydroxylase deficiency est un(e) (attribut) False Steroid 21-monooxygenase deficiency, simple virilising type Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start