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307116001: Heterozygous Factor V Leiden mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
450296019 Heterozygous Factor V Leiden mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
703598016 Heterozygous Factor V Leiden mutation (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

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 Existential restriction modifier
Heterozygous Factor V Leiden mutation Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Heterozygous Factor V Leiden mutation Finding site Body system structure false Inferred relationship Existential restriction modifier
Heterozygous Factor V Leiden mutation Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Heterozygous Factor V Leiden mutation Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Heterozygous Factor V Leiden mutation Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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