441420000: Homozygous prothrombin G20210A mutation (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Thrombophilia\Hereditary thrombophilia\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation
• \Disease\Disorder of haemostatic system\Thrombophilia\Hereditary thrombophilia\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation

Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2787282019	Homozygous prothrombin G20210A mutation (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2795461010	Homozygous prothrombin G20210A mutation	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start