Owren's disease (Q18452351)
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Human disease
- factor V deficiency
- Factor V deficiency (disorder)
- Factor V deficiency [Ambiguous]
- Hereditary hypoproaccelerinaemia
- Labile factor deficiency (disorder)
- Proaccelerin deficiency (disorder)
- deficiency, labile
- Labile factor deficiency
- Proaccelerin deficiency
- Owren disease
- FACTOR V DEFICIENCY
- Owren Parahemophilia
- Parahemophilia
- Hereditary Factor V Deficiency
Language | Label | Description | Also known as |
---|---|---|---|
English | Owren's disease |
Human disease |
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Statements
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4 references
C98938
2 references
1 reference
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Identifiers
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2 references
Sitelinks
Wikipedia(2 entries)
- kkwiki Оврен ауруы
- svwiki Owrens sjukdom