15991002: Severe steroid 21-hydroxylase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Viscus structure finding\Abdominal organ finding\Disorder of adrenal gland\Disorder of adrenal cortex\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Disorder of adrenal cortex\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Disorder of adrenal gland\Disorder of adrenal cortex\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Disorder of adrenal cortex\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Disorder of adrenal cortex\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Severe steroid 21-hydroxylase deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Severe steroid 21-hydroxylase deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Severe steroid 21-hydroxylase deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Severe steroid 21-hydroxylase deficiency
• \Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Severe steroid 21-hydroxylase deficiency
• \Disease\Disorder of body system\Disorder of endocrine system\Disorder of adrenal gland\Disorder of adrenal cortex\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Disorder of adrenal cortex\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Severe steroid 21-hydroxylase deficiency
• \Disease\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\Metabolic disease\Disorder of steroid metabolism\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\Congenital disease\Inborn error of metabolism\Severe steroid 21-hydroxylase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2006. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
27072017	Severe steroid 21-hydroxylase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
742926010	Severe steroid 21-hydroxylase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start