3760002: Familial multiple factor deficiency syndrome, type V (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Combined coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V
• \Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Combined coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V

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
7346016	Familial multiple factor deficiency syndrome, type V	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
7347013	FMFD syndrome, type V	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
7349011	Factors VIII, IX AND XI deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
769486010	Familial multiple factor deficiency syndrome, type V (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start