1336093007: Severe hereditary factor IX deficiency disease (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\Severe hereditary factor IX deficiency disease

\Hemophilia\Hereditary factor IX deficiency disease\Severe hereditary factor IX deficiency disease

\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease\Severe hereditary factor IX deficiency disease
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary factor IX deficiency disease\Severe hereditary factor IX deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease\Severe hereditary factor IX deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor IX deficiency disease\Severe hereditary factor IX deficiency disease

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5363309013 Severe hereditary factor IX deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363310015 Severe hereditary factor IX deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363311016 Severe hemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363312011 Severe haemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5363373013 A factor activity level <1 percent of normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Severe hereditary factor IX deficiency disease	Is a	Hereditary factor IX deficiency disease	true	Inferred relationship	Some
Severe hereditary factor IX deficiency disease	Occurrence	Congenital	true	Inferred relationship	Some	3
Severe hereditary factor IX deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Severe hereditary factor IX deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Severe hereditary factor IX deficiency disease	Severity	Severe	true	Inferred relationship	Some	2

Inbound Relationships

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This concept is not in any reference sets