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440866009: Severe hereditary factor IX deficiency disease with inhibitor (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2790023015 Severe hereditary factor IX deficiency disease with inhibitor (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2792952010 Severe hemophilia B with inhibitor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2792953017 Severe hereditary factor IX deficiency disease with inhibitor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2794297013 Severe haemophilia B with inhibitor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2503791000052119 svår ärftlig faktor IX-brist, med hämmare sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)
5211191000052110 svår ärftlig faktor IX-brist, med inhibitor sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe hereditary factor IX deficiency disease with inhibitor (disorder) Is a Hereditary factor IX deficiency disease with inhibitor (disorder) true Inferred relationship Some
Severe hereditary factor IX deficiency disease with inhibitor (disorder) Occurrence Congenital true Inferred relationship Some 2
Severe hereditary factor IX deficiency disease with inhibitor (disorder) Interprets Hemostatic function true Inferred relationship Some 1
Severe hereditary factor IX deficiency disease with inhibitor (disorder) Has interpretation Abnormal 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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