234445000: Congenital factor IX deficiency with inhibitor (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...

\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor

\Hemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor

\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor
\Disease\Congenital disease (disorder)\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

351267011 Congenital factor IX deficiency with inhibitor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
622764014 Congenital factor IX deficiency with inhibitor (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
146671000077119 déficience congénitale en facteur IX avec inhibiteur fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital factor IX deficiency with inhibitor	Is a	Hereditary factor IX deficiency disease	true	Inferred relationship	Some
Congenital factor IX deficiency with inhibitor	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Congenital factor IX deficiency with inhibitor	Is a	Congenital disease (disorder)	false	Inferred relationship	Some
Congenital factor IX deficiency with inhibitor	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital factor IX deficiency with inhibitor	Finding site	Body system structure	false	Inferred relationship	Some
Congenital factor IX deficiency with inhibitor	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Congenital factor IX deficiency with inhibitor	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Congenital factor IX deficiency with inhibitor	Interprets	Hemostatic function	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets