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438372000: 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
2787760013 Hereditary factor IX deficiency disease with inhibitor (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2791040019 Haemophilia B with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2791041015 Hemophilia B with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core
2791042010 Hereditary factor IX deficiency disease with inhibitor en Synonym Active Initial character case insensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Severe hereditary factor IX deficiency disease with inhibitor Is a True Hereditary factor IX deficiency disease with inhibitor Inferred relationship Some
Mild hereditary factor IX deficiency disease with inhibitor Is a True Hereditary factor IX deficiency disease with inhibitor Inferred relationship Some
Moderate hereditary factor IX deficiency disease with inhibitor Is a True Hereditary factor IX deficiency disease with inhibitor Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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