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439157002: Hereditary combined coagulation factor deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2787558013 Hereditary combined coagulation factor deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2795244014 Hereditary combined coagulation factor deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary combined coagulation factor deficiency Is a Combined coagulation factor deficiency true Inferred relationship Existential restriction modifier
Hereditary combined coagulation factor deficiency Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary combined coagulation factor deficiency Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Hereditary combined coagulation factor deficiency Is a Hereditary coagulation factor deficiency true Inferred relationship Existential restriction modifier

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

This concept is not in any reference sets

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