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41788008: Hereditary factor IX deficiency disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

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

11 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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