1336091009: Mild 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\Mild hereditary factor IX deficiency disease

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

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

5363301011 Mild hereditary factor IX deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363302016 Mild hemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363303014 Mild haemophilia B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363304015 Mild hereditary factor IX deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363368019 A factor activity level of >5 percent of normal and <40 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
Mild hereditary factor IX deficiency disease	Is a	Hereditary factor IX deficiency disease	true	Inferred relationship	Some
Mild hereditary factor IX deficiency disease	Occurrence	Congenital	true	Inferred relationship	Some	3
Mild hereditary factor IX deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease	Severity	Mild	true	Inferred relationship	Some	2

Inbound Relationships

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This concept is not in any reference sets