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439157002: Hereditary combined coagulation factor deficiency (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
2787558013 Hereditary combined coagulation factor deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2795244014 Hereditary combined coagulation factor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2425631000052110 ärftlig kombinerad koagulationsfaktorbrist sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary combined coagulation factor deficiency (disorder) Is a Combined coagulation factor deficiency true Inferred relationship Some
Hereditary combined coagulation factor deficiency (disorder) Interprets Hemostatic function true Inferred relationship Some 1
Hereditary combined coagulation factor deficiency (disorder) Has interpretation Abnormal true Inferred relationship Some 1
Hereditary combined coagulation factor deficiency (disorder) Is a Hereditary coagulation factor deficiency true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Combined deficiency of factor V and factor VIII (disorder) Is a True Hereditary combined coagulation factor deficiency (disorder) Inferred relationship Some
Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) Is a True Hereditary combined coagulation factor deficiency (disorder) Inferred relationship Some

This concept is not in any reference sets

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