28293008: Hereditary factor VIII deficiency disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...

\Factor VIII deficiency\Hereditary factor VIII deficiency disease

\Hemophilia\Hereditary factor VIII deficiency disease

\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease

\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor VIII deficiency disease
\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor VIII deficiency\Hereditary factor VIII deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor VIII deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VIII 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

47356012 Hemophilia A en Synonym Active Only initial character case insensitive SNOMED CT core module

47359017 Hereditary factor VIII deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module

47360010 Classical hemophilia en Synonym Active Entire term case insensitive SNOMED CT core module

47361014 AHG deficiency disease en Synonym Active Entire term case sensitive SNOMED CT core module

47362019 Sex-linked factor VIII deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

47363012 Congenital factor VIII deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module

483814018 Haemophilia A en Synonym Active Only initial character case insensitive SNOMED CT core module

483815017 Classical haemophilia en Synonym Active Entire term case insensitive SNOMED CT core module

1225870016 Congenital factor VIII deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

2787090010 Hereditary factor VIII 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 VIII deficiency disease	Is a	X-linked hereditary disease	true	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease	Is a	Hemophilia	true	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease	Is a	Hereditary coagulation factor deficiency	true	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease	Is a	Factor VIII deficiency	true	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	1
Hereditary factor VIII deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Carrier of hereditary factor VIII deficiency disease	Is a	False	Hereditary factor VIII deficiency disease	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease with inhibitor	Is a	True	Hereditary factor VIII deficiency disease	Inferred relationship	Existential restriction modifier
Severe hereditary factor VIII deficiency disease	Is a	True	Hereditary factor VIII deficiency disease	Inferred relationship	Existential restriction modifier
Mild hereditary factor VIII deficiency disease	Is a	True	Hereditary factor VIII deficiency disease	Inferred relationship	Existential restriction modifier
Moderate hereditary factor VIII deficiency disease	Is a	True	Hereditary factor VIII deficiency disease	Inferred relationship	Existential restriction modifier
Hereditary factor VIII deficiency disease without inhibitor	Is a	True	Hereditary factor VIII deficiency disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets