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440868005: Mild hereditary factor IX deficiency disease with inhibitor (disorder)


Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2790086014 Mild hereditary factor IX deficiency disease with inhibitor (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2791292015 Mild hemophilia B with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2793938017 Mild hereditary factor IX deficiency disease with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2794994014 Mild haemophilia B with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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