95841006: Hereditary hypoplasminogenemia (disorder)

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

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenemia (disorder)\Hereditary hypoplasminogenemia

\Disease\Genetic disease\Hereditary disease\Hereditary hypoplasminogenemia
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenemia (disorder)\Hereditary hypoplasminogenemia

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

158737014 Hereditary hypoplasminogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

512324012 Hereditary hypoplasminogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

840080012 Hereditary hypoplasminogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

158737014 Hereditary hypoplasminogenemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

158737014 Hereditary hypoplasminogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

512324012 Hereditary hypoplasminogenaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

512324012 Hereditary hypoplasminogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

840080012 Hereditary hypoplasminogenemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

840080012 Hereditary hypoplasminogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

345301000077115 hypoplasminogénémie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

345301000077115 hypoplasminogénémie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary hypoplasminogenemia	Is a	Hypoplasminogenemia (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Is a	Hereditary disorder of haematologic sysem	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Is a	Hereditary disorder by system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Is a	Hereditary disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary hypoplasminogenemia	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autosomal dominant deficiency of plasminogen	Is a	True	Hereditary hypoplasminogenemia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets