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717261006: Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder)


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

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 SNOMED CT core module
3308874019 Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


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 Due to 21-hydroxylase deficiency false Inferred relationship Existential restriction modifier
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Is a Congenital adrenal hyperplasia true Inferred relationship Existential restriction modifier
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Existential restriction modifier 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Steroid 21-monooxygenase deficiency, simple virilizing type Is a True Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, salt wasting type Is a True Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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