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41788008: Hereditary factor IX deficiency disease (disorder)

Status: current, Defined. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2786800010 Hereditary factor IX deficiency disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
493094016 Haemophilia B en Synonym Active Initial character case insensitive SNOMED CT core
493095015 Congenital factor IX deficiency en Synonym Active Initial character case insensitive SNOMED CT core
69707012 Hemophilia B en Synonym Active Initial character case insensitive SNOMED CT core
69709010 Hereditary factor IX deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core
69710017 Christmas disease en Synonym Active Case sensitive SNOMED CT core
69711018 Sex-linked factor IX deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core
69712013 PTC deficiency disease en Synonym Active Case sensitive SNOMED CT core

11 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary factor IX deficiency disease Has interpretation Abnormal true Inferred relationship Some 2
Hereditary factor IX deficiency disease Interprets Haemostatic function true Inferred relationship Some 2
Hereditary factor IX deficiency disease Is a X-linked hereditary disease true Inferred relationship Some
Hereditary factor IX deficiency disease Is a Haemophilia true Inferred relationship Some
Hereditary factor IX deficiency disease Is a Hereditary disorder of haematologic system false Inferred relationship Some
Hereditary factor IX deficiency disease Is a Hereditary disorder by system false Inferred relationship Some
Hereditary factor IX deficiency disease Finding site Body system structure false Inferred relationship Some
Hereditary factor IX deficiency disease Has definitional manifestation Haemostatic system finding false Inferred relationship Some
Hereditary factor IX deficiency disease Is a Hereditary coagulation factor deficiency false Inferred relationship Some
Hereditary factor IX deficiency disease Finding site Entire haematological system false Inferred relationship Some
Hereditary factor IX deficiency disease Occurrence Congenital true Inferred relationship Some 1
Hereditary factor IX deficiency disease Is a Congenital disease true Inferred relationship Some
Hereditary factor IX deficiency disease Is a Factor IX deficiency true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Acquired factor IX deficiency disease Is a False Hereditary factor IX deficiency disease Inferred relationship Some
Congenital factor IX deficiency without inhibitor Is a True Hereditary factor IX deficiency disease Inferred relationship Some
Hereditary factor IX deficiency disease without inhibitor Is a True Hereditary factor IX deficiency disease Inferred relationship Some
Hereditary factor IX deficiency disease with inhibitor Is a True Hereditary factor IX deficiency disease Inferred relationship Some
Congenital factor IX deficiency variant Is a True Hereditary factor IX deficiency disease Inferred relationship Some
Congenital factor IX deficiency with inhibitor Is a True Hereditary factor IX deficiency disease Inferred relationship Some

Reference Sets

Emergency department reference set

Australian emergency department reference set

NSW Emergency Department reference set

Clinical finding foundation reference set

Emergency department diagnosis reference set

Problem/Diagnosis reference set

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