237696003: Familial arginine vasopressin deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain\Disorder of pituitary gland (disorder)\Disorder of posterior pituitary\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Disorder of pituitary gland (disorder)\Disorder of posterior pituitary\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)

\Finding of body product\Polyuria\Arginine vasopressin-related polyuria (disorder)\...

\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)

\Familial vasopressin-related polyuria\Familial arginine vasopressin deficiency (disorder)

\Urine finding\Polyuria\Arginine vasopressin-related polyuria (disorder)\...

\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)

\Familial vasopressin-related polyuria\Familial arginine vasopressin deficiency (disorder)

\Central nervous system finding\Finding of brain\Disorder of brain\Disorder of pituitary gland (disorder)\Disorder of posterior pituitary\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Disorder of pituitary gland (disorder)\Disorder of posterior pituitary\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)

\Disease\Arginine vasopressin-related polyuria (disorder)\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)
\Disease\Arginine vasopressin-related polyuria (disorder)\Familial vasopressin-related polyuria\Familial arginine vasopressin deficiency (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of pituitary gland (disorder)\Disorder of posterior pituitary\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Disorder of pituitary gland (disorder)\Disorder of posterior pituitary\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain\Disorder of pituitary gland (disorder)\Disorder of posterior pituitary\Arginine vasopressin deficiency (disorder)\Familial arginine vasopressin deficiency (disorder)
\Disease\Familial disease\Familial vasopressin-related polyuria\Familial 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
Familial arginine vasopressin deficiency (disorder)	Is a	Arginine vasopressin deficiency (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial arginine vasopressin deficiency (disorder)	Is a	Familial vasopressin-related polyuria	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial arginine vasopressin deficiency (disorder)	Finding site	Pars nervosa of pituitary gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial arginine vasopressin deficiency (disorder)	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial arginine vasopressin deficiency (disorder)	Interprets	Nutritional deficiency state	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial arginine vasopressin deficiency (disorder)	Finding site	Neurohypophysis structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial arginine vasopressin deficiency (disorder)	Interprets	Urine output observable	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial arginine vasopressin deficiency (disorder)	Has interpretation	Increased	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autosomal dominant hereditary arginine vasopressin deficiency (disorder)	Is a	True	Familial arginine vasopressin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive hereditary arginine vasopressin deficiency (disorder)	Is a	True	Familial arginine vasopressin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
356246010	Familial central diabetes insipidus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5287681011	Familial vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5287682016	Familial arginine vasopressin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5289636019	Familial AVP-D (arginine vasopressin deficiency)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5289637011	Familial arginine vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
356246010	Familial central diabetes insipidus	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
356246010	Familial central diabetes insipidus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626462012	Familial central diabetes insipidus (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
626462012	Familial central diabetes insipidus (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5287681011	Familial vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5287682016	Familial arginine vasopressin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5289636019	Familial AVP-D (arginine vasopressin deficiency)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5289637011	Familial arginine vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6171011000241110	DIC (diabète insipide central) familial	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6171021000241115	diabète insipide familial d'origine centrale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6171011000241110	DIC (diabète insipide central) familial	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6171021000241115	diabète insipide familial d'origine centrale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module