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124221007: Deficiency of steroid 21-monooxygenase (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
203798012 Deficiency of steroid 21-hydroxylase en Synonym Active Entire term case insensitive SNOMED CT core module
203799016 Deficiency of steroid 21-monooxygenase en Synonym Active Entire term case insensitive SNOMED CT core module
473063012 CAH - 21-hydroxylase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
727726019 Deficiency of steroid 21-monooxygenase (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3332438012 21-hydroxylase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of steroid 21-monooxygenase Is a Specific enzyme deficiency true Inferred relationship Existential restriction modifier
Deficiency of steroid 21-monooxygenase Is a Congenital adrenal hyperplasia false Inferred relationship Existential restriction modifier
Deficiency of steroid 21-monooxygenase Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Deficiency of steroid 21-monooxygenase Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
Deficiency of steroid 21-monooxygenase Occurrence Congenital false Inferred relationship Existential restriction modifier
Deficiency of steroid 21-monooxygenase Is a Disorder of adrenal cortex true Inferred relationship Existential restriction modifier
Deficiency of steroid 21-monooxygenase Is a Disorder of steroid metabolism true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Severe steroid 21-hydroxylase deficiency Is a True Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier
Mild steroid 21-hydroxylase deficiency Is a True Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier
Moderate steroid 21-hydroxylase deficiency Is a True Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, salt wasting type Is a False Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Due to True Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier 2
Steroid 21-monooxygenase deficiency, salt wasting type Due to True Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier 2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Due to True Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier 2
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Due to True Deficiency of steroid 21-monooxygenase Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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