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1296897006: Autosomal hereditary arginine vasopressin resistance (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
5287683014 Autosomal hereditary arginine vasopressin resistance (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5287684015 Autosomal hereditary vasopressin resistance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5287690016 Hereditary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5289660015 Autosomal hereditary AVP-R (arginine vasopressin resistance) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5289661016 Autosomal hereditary arginine vasopressin resistance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5287683014 Autosomal hereditary arginine vasopressin resistance (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5287684015 Autosomal hereditary vasopressin resistance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5287690016 Hereditary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5289660015 Autosomal hereditary AVP-R (arginine vasopressin resistance) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5289661016 Autosomal hereditary arginine vasopressin resistance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal hereditary vasopressin resistance Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal hereditary vasopressin resistance Finding site Urinary system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal hereditary vasopressin resistance Interprets Urine output observable true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal hereditary vasopressin resistance Has interpretation Increased true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal hereditary vasopressin resistance Is a Hereditary arginine vasopressin resistance (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

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

This concept is not in any reference sets

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