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440866009: Severe 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
2790023015 Severe hereditary factor IX deficiency disease with inhibitor (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2792952010 Severe hemophilia B with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2792953017 Severe hereditary factor IX deficiency disease with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2794297013 Severe 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
Severe hereditary factor IX deficiency disease with inhibitor Interprets Haemostatic function true Inferred relationship Some 1
Severe hereditary factor IX deficiency disease with inhibitor Has interpretation Abnormal true Inferred relationship Some 1
Severe hereditary factor IX deficiency disease with inhibitor Is a Hereditary factor IX deficiency disease with inhibitor true Inferred relationship Some
Severe 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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