45369008: 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
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency

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

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

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency
\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

\Disease\Arginine vasopressin-related polyuria (disorder)\Vasopressin deficiency
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency
\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
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Disorder of posterior pituitary\Vasopressin deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Vasopressin deficiency	Is a	diabète insipide	false	Inferred relationship	Some
Vasopressin deficiency	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Vasopressin deficiency	Finding site	Neurohypophysis structure	true	Inferred relationship	Some	1
Vasopressin deficiency	Interprets	Nutritional deficiency (finding)	false	Inferred relationship	Some
Vasopressin deficiency	Interprets	Urine output observable	true	Inferred relationship	Some	2
Vasopressin deficiency	Has interpretation	Increased	true	Inferred relationship	Some	2
Vasopressin deficiency	Is a	Arginine vasopressin-related polyuria (disorder)	true	Inferred relationship	Some
Vasopressin deficiency	Is a	Disorder of posterior pituitary	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial vasopressin deficiency	Is a	True	Vasopressin deficiency	Inferred relationship	Some
Secondary arginine vasopressin-related polyuria (disorder)	Is a	False	Vasopressin deficiency	Inferred relationship	Some
Postoperative vasopressin deficiency	Is a	False	Vasopressin deficiency	Inferred relationship	Some
Arginine vasopressin deficiency due to trauma (disorder)	Is a	True	Vasopressin deficiency	Inferred relationship	Some
Secondary vasopressin deficiency	Is a	True	Vasopressin deficiency	Inferred relationship	Some
X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome is a rare genetic neurometabolic disease characterized by severe intellectual disability, spastic quadriparesis, Leber congenital amaurosis and diabetes insipidus. Additional manifestations include facial dysmorphy (dolichocephalic skull, hypertelorism, deep-set eyes, hypoplastic nares, low-set ears), short stature, truncal hypotonia and axial hypertonia. Brain anomalies (e.g. thin corpus callosum with lack of isthmus and tapered splenium, hypoplasia or atrophy of the optic chiasm, prominent lateral ventricles, diminished white matter), described on magnetic resonance imaging, have been reported. High prenatal alpha-fetoprotein and intrauterine growth restriction is observed in routine pregnancy examination.	Is a	True	Vasopressin deficiency	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
75633018	Neurohypophyseal diabetes insipidus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
75635013	Pituitary diabetes insipidus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
75637017	Neurogenic diabetes insipidus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
75638010	Cranial diabetes insipidus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
494186019	Diabetes insipidus - pituitary	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
494187011	Vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
494188018	Central diabetes insipidus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5287215017	Arginine vasopressin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5287216016	AVP-D - arginine vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5289693012	Arginine vasopressin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1826401000195118	carenza di arginina vasopressina	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
465331000172119	diabète insipide hypophysaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3386421001000118	Diabetes insipidus, zentraler	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module