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237696003: 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:

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
2985521000005110 familiær central diabetes insipidus da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) dansk modul


2 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant hereditary arginine vasopressin deficiency (disorder) Is a True Familial vasopressin deficiency Inferred relationship Some
Autosomal recessive hereditary arginine vasopressin deficiency (disorder) Is a True Familial vasopressin deficiency Inferred relationship Some

This concept is not in any reference sets

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