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717261006: klassieke congenitale bijnierhyperplasie door 21-hydroxylasedeficiëntie (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
3308873013 Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308874019 Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6200401000146118 klassieke congenitale bijnierhyperplasie door 21-hydroxylasedeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6200411000146116 klassieke congenitale bijnierhyperplasie door 21-hydroxylasedeficiëntie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6200421000146114 klassieke congenitale adrenale hyperplasie door 21-hydroxylasedeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3308875018 The most common form of congenital adrenal hyperplasia, divided into 2 clinical groups simple virilizing or salt wasting forms. Manifests with genital ambiguity in females and with adrenal insufficiency in both sexes. Girls present with ambiguous genitalia and the extent of virilization can vary from a nearly male appearance to minimal clitoromegaly. A normal uterus and various degrees of abnormal vaginal development are seen. The external genitalia in boys are normal. The disease is caused by a mutation in the CYP21A2 gene located on chromosome 6p21.3. Follows an autosomal recessive pattern of inheritance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308876017 The most common form of congenital adrenal hyperplasia, divided into 2 clinical groups simple virilising or salt wasting forms. Manifests with genital ambiguity in females and with adrenal insufficiency in both sexes. Girls present with ambiguous genitalia and the extent of virilisation can vary from a nearly male appearance to minimal clitoromegaly. A normal uterus and various degrees of abnormal vaginal development are seen. The external genitalia in boys are normal. The disease is caused by a mutation in the CYP21A2 gene located on chromosome 6p21.3. Follows an autosomal recessive pattern of inheritance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Due to 21-hydroxylase deficiency false Inferred relationship Some
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Is a Congenital adrenal hyperplasia true Inferred relationship Some
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Associated morphology congenitale hyperplasie false Inferred relationship Some 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Occurrence Congenital false Inferred relationship Some 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Finding site Adrenal cortex structure false Inferred relationship Some 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Some 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Finding site Adrenal cortex structure true Inferred relationship Some 1
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Occurrence Congenital true Inferred relationship Some 1
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Associated morphology Hyperplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Steroid 21-monooxygenase deficiency, simple virilising type Is a True Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Inferred relationship Some
Steroid 21-monooxygenase deficiency, salt wasting type Is a True Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) Inferred relationship Some

This concept is not in any reference sets

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