15991002: Severe steroid 21-hydroxylase deficiency (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Viscus structure finding (finding)\constatation à propos d'un organe abdominal\Disorder of adrenal gland (disorder)\Disorder of adrenal cortex (disorder)\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland (disorder)\Disorder of adrenal cortex (disorder)\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\constatation à propos d'un organe abdominal\Disorder of adrenal gland (disorder)\Disorder of adrenal cortex (disorder)\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland (disorder)\Disorder of adrenal cortex (disorder)\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland (disorder)\Disorder of adrenal cortex (disorder)\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Severe steroid 21-hydroxylase deficiency
• \Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Severe steroid 21-hydroxylase deficiency
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Severe steroid 21-hydroxylase deficiency
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Severe steroid 21-hydroxylase deficiency
• \Disease\affection d'un système corporel\pathologie endocrinologique\Hereditary disorder of endocrine system (disorder)\Severe steroid 21-hydroxylase deficiency
• \Disease\affection d'un système corporel\pathologie endocrinologique\Disorder of adrenal gland (disorder)\Disorder of adrenal cortex (disorder)\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland (disorder)\Disorder of adrenal cortex (disorder)\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\trouble métabolique\Inborn error of metabolism\Severe steroid 21-hydroxylase deficiency
• \Disease\trouble métabolique\Enzymopathy\Specific enzyme deficiency\Deficiency of steroid 21-monooxygenase\Severe steroid 21-hydroxylase deficiency
• \Disease\trouble métabolique\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 (core metadata concept). Date: 31-Jul 2006. Module: SNOMED CT core

Descriptions:

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

Expanded Value Set

This concept is not in any reference sets

Back to Start