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26029002: Mild hereditary factor VIII deficiency disease (disorder)


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
43600019 Mild hemophilia A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483093012 Mild haemophilia A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2787929017 Mild hereditary factor VIII deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2792392016 Mild hereditary factor VIII deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2884517012 Mild disease manifests factor VIII activity of greater than 5% of normal en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
43600019 Mild hemophilia A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
43601015 6-60% of normal factor VIII en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
483093012 Mild haemophilia A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
756414016 Mild hemophilia A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2787929017 Mild hereditary factor VIII deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2792392016 Mild hereditary factor VIII deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2884517012 Mild disease manifests factor VIII activity of greater than 5% of normal en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3420811001000113 Hämophilie A, milde de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6495231000241118 déficit héréditaire léger en facteur VIII de la coagulation fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6495251000241114 hémophilie A légère fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6495271000241116 déficit héréditaire léger en facteur antihémophilique A fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6495231000241118 déficit héréditaire léger en facteur VIII de la coagulation fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6495251000241114 hémophilie A légère fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6495271000241116 déficit héréditaire léger en facteur antihémophilique A fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3420811001000113 Hämophilie A, milde de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mild haemophilia A Is a Hemophilia A true Inferred relationship Existential restriction modifier (core metadata concept)
Mild haemophilia A Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Mild haemophilia A Severity Mild false Inferred relationship Existential restriction modifier (core metadata concept)
Mild haemophilia A Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Mild haemophilia A Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Mild haemophilia A Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 1
Mild haemophilia A Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Mild hemophilia A with inhibitor Is a True Mild haemophilia A Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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