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41788008: Hereditary factor IX deficiency disease (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
69707012 Hemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
69708019 Hemophilia B, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
69709010 Hereditary factor IX deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
69710017 Christmas disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
69711018 Sex-linked factor IX deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
69712013 PTC deficiency disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
69713015 Haemophilia B, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
197592013 Factor IX deficiency en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
493094016 Haemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
493095015 Congenital factor IX deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
778615016 Hemophilia B (disorder) en Fully specified name Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
2786800010 Hereditary factor IX deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

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 Some
Hereditary factor IX deficiency disease Is a Hemophilia true Inferred relationship Some
Hereditary factor IX deficiency disease Is a Hereditary disorder of hematologic system false Inferred relationship Some
Hereditary factor IX deficiency disease Finding site Entire hematological system (body structure) 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 Hemostatic 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 Occurrence Congenital true Inferred relationship Some 1
Hereditary factor IX deficiency disease Is a Congenital disease (disorder) true Inferred relationship Some
Hereditary factor IX deficiency disease Is a Factor IX deficiency (disorder) true Inferred relationship Some
Hereditary factor IX deficiency disease Has interpretation Abnormal true Inferred relationship Some 2
Hereditary factor IX deficiency disease Interprets Hemostatic function true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
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
Acquired factor IX deficiency disease Is a False Hereditary factor IX deficiency disease Inferred relationship Some
Congenital factor IX deficiency without inhibitor (disorder) Is a True Hereditary factor IX deficiency disease Inferred relationship Some
Hereditary factor IX deficiency disease without inhibitor (disorder) Is a True Hereditary factor IX deficiency disease Inferred relationship Some
Hereditary factor IX deficiency disease with inhibitor (disorder) Is a True Hereditary factor IX deficiency disease Inferred relationship Some

This concept is not in any reference sets

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