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71578002: 21-hydroxylasedeficiëntie met zoutverlies (aandoening)


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
6267471000146113 21-hydroxylasedeficiëntie met zoutverlies nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267481000146110 21-hydroxylasedeficiëntie met zoutverlies (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267491000146112 zoutverliezende vorm van 21-hydroxylasedeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267551000146118 congenitale bijnierhyperplasie type 2 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267561000146115 CAH type 2 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267571000146114 adrenogenitaal syndroom type 2 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267581000146111 AGS type 2 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Steroid 21-monooxygenase deficiency, salt wasting type Is a Salt-losing congenital adrenal hyperplasia true Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Finding site Adrenal cortex structure false Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Associated morphology congenitale hyperplasie false Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type Occurrence Congenital false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Is a Deficiency of steroid 21-monooxygenase false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Associated morphology Hyperplasia true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type Is a Congenital anomaly of adrenal gland (disorder) false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Associated morphology congenitale hyperplasie false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, salt wasting type Finding site Adrenal cortex structure false Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type Occurrence Congenital false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, salt wasting type Associated morphology Hyperplasia false Inferred relationship Some 2
Steroid 21-monooxygenase deficiency, salt wasting type Finding site Adrenal cortex structure false Inferred relationship Some 3
Steroid 21-monooxygenase deficiency, salt wasting type Occurrence Congenital true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type Finding site Adrenal cortex structure true Inferred relationship Some 1
Steroid 21-monooxygenase deficiency, salt wasting type Due to 21-hydroxylase deficiency false Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Is a Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) 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 Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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