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35105006: Increased (qualifier value)

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

Descriptions:

Id Description Lang Type Status Case? Module
58584013 Increased en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
58585014 Augmented en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
58586010 Increased by en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
766708012 Increased (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Increased Is a Degree findings true Inferred relationship Some
Increased Is a General adjectival modifier false Inferred relationship Some
Increased Is a Changed status (qualifier value) true Inferred relationship Some
Increased Is a Descriptor (qualifier value) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary vasopressin resistance Has interpretation True Increased Inferred relationship Some 1
Autosomal dominant hereditary arginine vasopressin resistance (disorder) Has interpretation True Increased Inferred relationship Some 1
Autosomal recessive hereditary arginine vasopressin resistance (disorder) Has interpretation True Increased Inferred relationship Some 1
X-linked hereditary vasopressin resistance Has interpretation True Increased Inferred relationship Some 1
Partial vasopressin-related polyuria Has interpretation True Increased Inferred relationship Some 1
Idiopathic arginine vasopressin-related polyuria (disorder) Has interpretation True Increased Inferred relationship Some 1
Hereditary arginine vasopressin-related polyuria (disorder) Has interpretation True Increased Inferred relationship Some 1
Autosomal dominant hereditary arginine vasopressin deficiency (disorder) Has interpretation True Increased Inferred relationship Some 1
Autosomal recessive hereditary arginine vasopressin deficiency (disorder) Has interpretation True Increased Inferred relationship Some 1
Secondary vasopressin deficiency Has interpretation True Increased Inferred relationship Some 1
Secondary arginine vasopressin resistance (disorder) Has interpretation True Increased Inferred relationship Some 1
Panhypophysitis (disorder) Has interpretation True Increased Inferred relationship Some 3
Adipsic arginine vasopressin-related polyuria (disorder) Has interpretation True Increased Inferred relationship Some 2
Hypohidrosis-diabetes insipidus syndrome Has interpretation True Increased Inferred relationship Some 4
Organic primary polydipsia (disorder) Has interpretation True Increased Inferred relationship Some 2
Psychogenic polydipsia Has interpretation True Increased Inferred relationship Some 2
At increased risk for maternal perinatal disorder Has interpretation True Increased Inferred relationship Some 1
Postural orthostatic tachycardia syndrome (disorder) Has interpretation True Increased Inferred relationship Some 2
Postural orthostatic tachycardia syndrome due to norepinephrine transporter deficiency Has interpretation True Increased Inferred relationship Some 3
Bier anemic spots, cyanosis, and urticaria-like eruption syndrome (disorder) Has interpretation True Increased Inferred relationship Some 4

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This concept is not in any reference sets

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