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47757001: Corticosterone 18-monooxygenase deficiency (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
79583012 Corticosterone 18-monooxygenase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
79584018 18-Hydroxylase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
79585017 Aldosterone deficiency due to 18-hydroxylase defect en Synonym Active Entire term case insensitive SNOMED CT core module
79586016 Corticosterone methyl oxidase type I deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
79587013 CMO I deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
494915012 CMO II deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
494916013 Corticosterone methyl oxidase type II deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
494917016 18-Hydroxycorticosterone dehydrogenase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
494918014 Aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
494919018 CAH - 18-hydroxylase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
785250014 Corticosterone 18-monooxygenase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Corticosterone 18-monooxygenase deficiency Is a Congenital adrenal hyperplasia true Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Reproductive system hereditary disorder false Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Enzymopathy true Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Hereditary disorder of endocrine system false Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Disorder of steroid metabolism true Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Aldosterone deficiency true Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Is a Congenital anomaly of adrenal gland false Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 1
Corticosterone 18-monooxygenase deficiency Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Corticosterone 18-monooxygenase deficiency Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier 1
Corticosterone 18-monooxygenase deficiency Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier 1
Corticosterone 18-monooxygenase deficiency Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1
Corticosterone 18-monooxygenase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Corticosterone 18-monooxygenase deficiency Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier 2
Corticosterone 18-monooxygenase deficiency Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
Corticosterone 18-monooxygenase deficiency Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 1
Corticosterone 18-monooxygenase deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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