1336117005: Hemophilia B Leyden (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\Hemophilia B Leyden (disorder)

\Hemophilia\Hereditary factor IX deficiency disease\Hemophilia B Leyden (disorder)

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

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

5363476018 Hemophilia B Leyden (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363477010 Haemophilia B Leyden en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363478017 Factor 9 deficiency Leyden type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363479013 Factor IX deficiency Leyden type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5363480011 Hemophilia B Leyden en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemophilia B Leyden (disorder)	Is a	Hereditary factor IX deficiency disease	true	Inferred relationship	Some
Hemophilia B Leyden (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Hemophilia B Leyden (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hemophilia B Leyden (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hemophilia B Leyden (disorder)	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets