31925001: Hereditary factor I deficiency disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...

\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease

\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
\Disease\Congenital disease\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease

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

53348015 Hereditary factor I deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module
53349011 Hereditary factor I deficiency disease, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
53350011 Hereditary hypofibrinogenemia en Synonym Active Entire term case insensitive SNOMED CT core module
53351010 Congenital hypofibrinogenemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
53352015 Congenital afibrinogenemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
485078010 Congenital afibrinogenaemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
485079019 Congenital hypofibrinogenaemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
485080016 Hereditary hypofibrinogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module
763149014 Hereditary factor I deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor I deficiency disease	Is a	Hereditary coagulation factor deficiency	false	Inferred relationship	Existential restriction modifier
Hereditary factor I deficiency disease	Is a	Congenital fibrinogen abnormality	true	Inferred relationship	Existential restriction modifier
Hereditary factor I deficiency disease	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier
Hereditary factor I deficiency disease	Is a	Factor XIII deficiency disease	false	Inferred relationship	Existential restriction modifier
Hereditary factor I deficiency disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Hereditary factor I deficiency disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hereditary factor I deficiency disease	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Existential restriction modifier
Hereditary factor I deficiency disease	Is a	Hereditary coagulation factor deficiency	true	Inferred relationship	Existential restriction modifier
Hereditary factor I deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	2
Hereditary factor I deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital hypofibrinogenemia	Is a	True	Hereditary factor I deficiency disease	Inferred relationship	Existential restriction modifier
Hereditary dysfibrinogenemia	Is a	True	Hereditary factor I deficiency disease	Inferred relationship	Existential restriction modifier
Congenital afibrinogenemia	Is a	True	Hereditary factor I deficiency disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets