1296914004: Autosomal dominant hereditary arginine vasopressin deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Finding of body product\Polyuria (finding)\Arginine vasopressin-related polyuria (disorder)\...
• \Hereditary arginine vasopressin-related polyuria (disorder)\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Familial vasopressin-related polyuria\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Urine finding\Polyuria (finding)\Arginine vasopressin-related polyuria (disorder)\...
• \Hereditary arginine vasopressin-related polyuria (disorder)\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Familial vasopressin-related polyuria\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Arginine vasopressin-related polyuria (disorder)\Hereditary arginine vasopressin-related polyuria (disorder)\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Arginine vasopressin-related polyuria (disorder)\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Arginine vasopressin-related polyuria (disorder)\Familial vasopressin-related polyuria\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary arginine vasopressin-related polyuria (disorder)\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system (disorder)\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)
• \Disease\Familial disease\Familial vasopressin-related polyuria\Familial vasopressin deficiency\Autosomal dominant hereditary arginine vasopressin deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5287802016	Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5287803014	Autosomal dominant hereditary arginine vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5289653014	Autosomal dominant hereditary vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5289654015	Autosomal dominant hereditary AVP-D (arginine vasopressin deficiency)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

GB English

US English

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