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

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

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\...

\Combined coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V (disorder)

\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V (disorder)
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Combined coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V (disorder)
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type V (disorder)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial multiple factor deficiency syndrome, type V (disorder)	Is a	Familial multiple factor deficiency syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type V (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type V (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type V (disorder)	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type V (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial multiple factor deficiency syndrome, type V (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
7346016	Familial multiple factor deficiency syndrome, type V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7347013	FMFD syndrome, type V	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
7349011	Factors VIII, IX AND XI deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
769486010	Familial multiple factor deficiency syndrome, type V (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7346016	Familial multiple factor deficiency syndrome, type V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7347013	FMFD syndrome, type V	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
7349011	Factors VIII, IX AND XI deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
769486010	Familial multiple factor deficiency syndrome, type V (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6189521000241119	syndrome familial de déficit combiné en facteurs de coagulation, type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6189531000241117	déficit combiné en facteurs VIII, IX et XI	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6189541000241110	syndrome familial de déficits multiples en facteurs de coagulation, type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6189521000241119	syndrome familial de déficit combiné en facteurs de coagulation, type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6189531000241117	déficit combiné en facteurs VIII, IX et XI	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6189541000241110	syndrome familial de déficits multiples en facteurs de coagulation, type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module