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1296911007: hereditaire arginine-vasopressinegerelateerde polyurie (aandoening)

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
5287792016 Hereditary arginine vasopressin-related polyuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5287793014 Hereditary arginine vasopressin-related polyuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5289639014 Hereditary vasopressin-related polyuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5289646017 Hereditary AVP (arginine vasopressin)-related polyuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
14893751000146119 hereditaire arginine-vasopressinegerelateerde polyurie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14893761000146116 hereditaire AVP-gerelateerde polyurie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14893771000146110 hereditaire arginine-vasopressinegerelateerde polyurie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14893781000146112 erfelijke diabetes insipidus nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary arginine vasopressin-related polyuria (disorder) Is a Arginine vasopressin-related polyuria (disorder) true Inferred relationship Some
Hereditary arginine vasopressin-related polyuria (disorder) Is a Hereditary disease true Inferred relationship Some
Hereditary arginine vasopressin-related polyuria (disorder) Interprets Urine output observable true Inferred relationship Some 1
Hereditary arginine vasopressin-related polyuria (disorder) Has interpretation Increased true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary vasopressin resistance Is a True Hereditary arginine vasopressin-related polyuria (disorder) Inferred relationship Some
Autosomal dominant hereditary arginine vasopressin deficiency (disorder) Is a True Hereditary arginine vasopressin-related polyuria (disorder) Inferred relationship Some
Autosomal recessive hereditary arginine vasopressin deficiency (disorder) Is a True Hereditary arginine vasopressin-related polyuria (disorder) Inferred relationship Some
X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder) Is a True Hereditary arginine vasopressin-related polyuria (disorder) Inferred relationship Some

This concept is not in any reference sets

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