307116001: Heterozygous Factor V Leiden mutation (disorder)

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

\Functional finding\Thrombophilia\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Heterozygous Factor V Leiden mutation

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Heterozygous Factor V Leiden mutation
\Disease\Thrombophilia\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Heterozygous Factor V Leiden mutation

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

450296019 Heterozygous Factor V Leiden mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) IPS terminology module (core metadata concept)

703598016 Heterozygous Factor V Leiden mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) IPS terminology module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Heterozygous Factor V Leiden mutation	Is a	Factor V Leiden mutation	true	Inferred relationship	Some
Heterozygous Factor V Leiden mutation	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Heterozygous Factor V Leiden mutation	Interprets	Hemostatic function	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

International Patient Summary