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1336092002: matige hereditaire stollingsfactor IX-deficiëntieziekte (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5363305019 Moderate hereditary factor IX deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363306018 Moderate hereditary factor IX deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363307010 Moderate haemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363308017 Moderate hemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
15015361000146110 matige hemofilie B nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15015371000146116 matige hereditaire stollingsfactor IX-deficiëntieziekte (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15015381000146119 matige hereditaire stollingsfactor IX-deficiëntieziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15015391000146117 matige erfelijke factor IX-deficiëntieziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5363369010 A factor activity level ≥1 percent of normal and ≤5 percent of normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Moderate hereditary factor IX deficiency disease (disorder) Is a Hereditary factor IX deficiency disease true Inferred relationship Some
Moderate hereditary factor IX deficiency disease (disorder) Occurrence Congenital true Inferred relationship Some 3
Moderate hereditary factor IX deficiency disease (disorder) Interprets Hemostatic function true Inferred relationship Some 1
Moderate hereditary factor IX deficiency disease (disorder) Has interpretation Abnormal true Inferred relationship Some 1
Moderate hereditary factor IX deficiency disease (disorder) Severity Moderate (severity modifier) (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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