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7391009: dragerschap van hereditaire aanleg voor hemoglobine-D-ziekte (aandoening)


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
13181013 Hemoglobin D trait en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
13182018 Hemoglobin D-A disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
502562017 Heterozygous for Hb D en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
502563010 Haemoglobin D-A disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
502564016 Haemoglobin D trait en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
814351014 Hemoglobin D trait (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3654671000146119 dragerschap van erfelijke aanleg voor hemoglobine-D-ziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3654681000146117 drager van HbD-ziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3654721000146111 heterozygoot voor hemoglobine-D-ziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8617511000146114 dragerschap van hereditaire aanleg voor hemoglobine-D-ziekte (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8647631000146113 dragerschap van hereditaire aanleg voor hemoglobine-D-ziekte nl Synonym (core metadata concept) 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
Hemoglobin D trait Is a Hereditary haemoglobinopathy due to globin chain mutation true Inferred relationship Some
Hemoglobin D trait Finding site Hematopoietic system structure false Inferred relationship Some
Hemoglobin D trait Finding site Erythrocyte false Inferred relationship Some
Hemoglobin D trait Finding site Hematopoietic system structure false Inferred relationship Some
Hemoglobin D trait Has definitional manifestation Red blood cell finding false Inferred relationship Some
Hemoglobin D trait Finding site Body system structure false Inferred relationship Some
Hemoglobin D trait Is a Heterozygous hemoglobinopathy true Inferred relationship Some
Hemoglobin D trait Occurrence Congenital true Inferred relationship Some 1
Hemoglobin D trait Finding site Erythrocyte true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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