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124220008: Deficiency of steroid 17-alpha-monooxygenase (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
203795010 Deficiency of steroid 17-alpha-hydroxylase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
203796011 Deficiency of steroid 17-alpha-monooxygenase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473057015 Congenital adrenal hyperplasia, type 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473058013 Adrenogenital disorder due to 17-alpha-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473059017 Steroid 17-alpha-monooxygenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473060010 CAH - 17-alpha-hydroxysteroid dehydrogenase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
473061014 CAH - 17-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
473062019 17 alpha-Hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
727724016 Deficiency of steroid 17-alpha-monooxygenase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
203795010 Deficiency of steroid 17-alpha-hydroxylase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
203795010 Deficiency of steroid 17-alpha-hydroxylase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
203796011 Deficiency of steroid 17-alpha-monooxygenase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
203796011 Deficiency of steroid 17-alpha-monooxygenase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473057015 Congenital adrenal hyperplasia, type 5 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
473057015 Congenital adrenal hyperplasia, type 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473058013 Adrenogenital disorder due to 17-alpha-hydroxylase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
473058013 Adrenogenital disorder due to 17-alpha-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473059017 Steroid 17-alpha-monooxygenase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
473059017 Steroid 17-alpha-monooxygenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473060010 CAH - 17-alpha-hydroxysteroid dehydrogenase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
473061014 CAH - 17-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
473062019 17 alpha-Hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
727724016 Deficiency of steroid 17-alpha-monooxygenase (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
727724016 Deficiency of steroid 17-alpha-monooxygenase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3451241001000118 Nebennierenhyperplasie, kongenitale, durch 17-alpha-Hydroxylase-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4770561000241110 déficit en steroid 17-alpha-monooxygénase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4770561000241110 déficit en steroid 17-alpha-monooxygénase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3451241001000118 Nebennierenhyperplasie, kongenitale, durch 17-alpha-Hydroxylase-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of steroid 17-alpha-monooxygenase Is a Specific enzyme deficiency true Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of steroid 17-alpha-monooxygenase Is a Congenital adrenal hyperplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of steroid 17-alpha-monooxygenase Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Deficiency of steroid 17-alpha-monooxygenase Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of steroid 17-alpha-monooxygenase Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of steroid 17-alpha-monooxygenase Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Deficiency of steroid 17-alpha-monooxygenase Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Deficiency of steroid 17-alpha-monooxygenase Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deficiency of steroid 17-alpha-monooxygenase Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deficiency of steroid 17-alpha-monooxygenase Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Deficiency of steroid 17-alpha-monooxygenase Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deficiency of steroid 17-alpha-monooxygenase Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Deficiency of steroid 17-alpha-monooxygenase Pathological process (attribute) Pathological developmental process (qualifier value) 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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