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441190003: Severe hereditary factor IX deficiency disease without inhibitor (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2789418016 Severe hereditary factor IX deficiency disease without inhibitor (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2792427019 Severe haemophilia B without inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2794172017 Severe hereditary factor IX deficiency disease without inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2794173010 Severe hemophilia B without 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 without inhibitor Interprets Haemostatic function true Inferred relationship Some 1
Severe hereditary factor IX deficiency disease without inhibitor Has interpretation Abnormal true Inferred relationship Some 1
Severe hereditary factor IX deficiency disease without inhibitor Is a Hereditary factor IX deficiency disease without inhibitor true Inferred relationship Some
Severe hereditary factor IX deficiency disease without 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

Australian dialect reference set

Problem/Diagnosis reference set

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