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1336117005: hereditaire stollingsfactor IX-deficiëntie van Leyden-type (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
5363476018 Hemophilia B Leyden (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363477010 Haemophilia B Leyden en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363478017 Factor 9 deficiency Leyden type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363479013 Factor IX deficiency Leyden type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363480011 Hemophilia B Leyden en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
15013451000146117 erfelijke factor IX-deficiëntie type Leyden nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15013461000146119 hereditaire stollingsfactor IX-deficiëntie van Leyden-type nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15013471000146113 hemofilie B van Leyden-type nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15013481000146110 hereditaire stollingsfactor IX-deficiëntie van Leyden-type (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemophilia B Leyden (disorder) Is a Hereditary factor IX deficiency disease true Inferred relationship Some
Hemophilia B Leyden (disorder) Occurrence Congenital true Inferred relationship Some 2
Hemophilia B Leyden (disorder) Interprets Hemostatic function true Inferred relationship Some 1
Hemophilia B Leyden (disorder) Has interpretation Abnormal true Inferred relationship Some 1
Hemophilia B Leyden (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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