37350004: Hereditary factor X deficiency disease (disorder)

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

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...

\Prothrombin complex deficiency\Factor X deficiency\Hereditary factor X deficiency disease

\Coagulation factor deficiency syndrome\Factor X deficiency\Hereditary factor X deficiency disease
\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor X deficiency disease

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor X deficiency disease
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor X deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Prothrombin complex deficiency\Factor X deficiency\Hereditary factor X deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor X deficiency\Hereditary factor X deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor X deficiency disease

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

62309012 Hereditary factor X deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

62310019 Hereditary Stuart factor deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

62311015 Hereditary Stuart-Prower deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

769207019 Hereditary factor X deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2032391000052116 ärftlig faktor X-brist sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor X deficiency disease	Is a	Factor X deficiency	true	Inferred relationship	Some
Hereditary factor X deficiency disease	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Hereditary factor X deficiency disease	Is a	Hereditary coagulation factor deficiency	true	Inferred relationship	Some
Hereditary factor X deficiency disease	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary factor X deficiency disease	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary factor X deficiency disease	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary factor X deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary factor X deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Prevention of bleeding in hereditary factor X deficiency disease	Has focus	False	Hereditary factor X deficiency disease	Inferred relationship	Some	2
Bleeding due to hereditary factor X deficiency disease (finding)	Due to	True	Hereditary factor X deficiency disease	Inferred relationship	Some	2

This concept is not in any reference sets