1296914004: autosomaal dominante hereditaire arginine-vasopressinedeficiëntie (aandoening)

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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Is a	Hereditary arginine vasopressin-related polyuria (disorder)	true	Inferred relationship	Some
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Is a	Hereditary disorder of endocrine system (disorder)	true	Inferred relationship	Some
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Finding site	Neurohypophysis structure	true	Inferred relationship	Some	2
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Interprets	Urine output observable	true	Inferred relationship	Some	1
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Has interpretation	Increased	true	Inferred relationship	Some	1
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Is a	Familial vasopressin deficiency	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
14893241000146110	autosomaal dominante hereditaire arginine-vasopressinedeficiëntie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14893251000146113	autosomaal dominante erfelijke centrale diabetes insipidus	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14893261000146111	autosomaal dominante hereditaire arginine-vasopressinedeficiëntie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)