307115002: Homozygous Factor V Leiden mutation (disorder)

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

\Functional finding\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Homozygous Factor V Leiden mutation

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Homozygous Factor V Leiden mutation
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Homozygous Factor V Leiden mutation

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

450295015 Homozygous Factor V Leiden mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

703597014 Homozygous Factor V Leiden mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous Factor V Leiden mutation	Is a	Factor V Leiden mutation	true	Inferred relationship	Some
Homozygous Factor V Leiden mutation	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Homozygous Factor V Leiden mutation	Finding site	Body system structure	false	Inferred relationship	Some
Homozygous Factor V Leiden mutation	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Homozygous Factor V Leiden mutation	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Homozygous Factor V Leiden mutation	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets