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52604008: Steroid 21-monooxygenase deficiency, simple virilizing type (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
87546013 Steroid 21-monooxygenase deficiency, simple virilizing type en Synonym Active Entire term case insensitive SNOMED CT core module
87547016 Steroid 21-hydroxylase deficiency en Synonym Inactive Only initial character case insensitive SNOMED CT core module
87548014 Simple virilizing adrenal hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
87549018 Adrenogenital disorder due to 21-hydroxylase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
87550018 Congenital adrenal hyperplasia, type 1 en Synonym Active Entire term case insensitive SNOMED CT core module
198397017 Steroid 21-hydroxylase deficiency, simiple virilizing type en Synonym Inactive Only initial character case insensitive SNOMED CT core module
496368011 Steroid 21-monooxygenase deficiency, simple virilising type en Synonym Active Entire term case insensitive SNOMED CT core module
496369015 Simple-virilising congenital adrenal hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
496370019 Simple virilising adrenal hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
496371015 Steroid 21-hydroxylase deficiency, simiple virilising type en Synonym Inactive Only initial character case insensitive SNOMED CT core module
496372010 Simple-virilizing congenital adrenal hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
790632010 Steroid 21-monooxygenase deficiency, simple virilizing type (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1783827016 Steroid 21-hydroxylase deficiency, simple virilising type en Synonym Active Entire term case insensitive SNOMED CT core module
1784215016 Steroid 21-hydroxylase deficiency, simple virilizing type en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Congenital anomaly of adrenal gland false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Inborn error of metabolism false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Adrenal virilism false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Enzymopathy false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Hereditary disorder of endocrine system false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Congenital adrenal hyperplasia false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Reproductive system hereditary disorder false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 1
Steroid 21-monooxygenase deficiency, simple virilizing type Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Occurrence Congenital false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 1
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Virilizing syndrome of adrenal origin true Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Disorder of steroid metabolism false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 3
Steroid 21-monooxygenase deficiency, simple virilizing type Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 1
Steroid 21-monooxygenase deficiency, simple virilizing type Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Steroid 21-monooxygenase deficiency, simple virilizing type Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier 2
Steroid 21-monooxygenase deficiency, simple virilizing type Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 3
Steroid 21-monooxygenase deficiency, simple virilizing type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Steroid 21-monooxygenase deficiency, simple virilizing type Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
Steroid 21-monooxygenase deficiency, simple virilizing type Due to 21-hydroxylase deficiency false Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Is a Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency true Inferred relationship Existential restriction modifier
Steroid 21-monooxygenase deficiency, simple virilizing type Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Existential restriction modifier 2
Steroid 21-monooxygenase deficiency, simple virilizing type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Steroid 21-monooxygenase deficiency, simple virilizing type Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Mild steroid 21-hydroxylase deficiency Is a False Steroid 21-monooxygenase deficiency, simple virilizing type Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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