Diehtu doahpagis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Ávžžuhuvvon tearbma
Factor V Deficiency
Tiipa
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Topical Descriptor
Badjedoaba
Stivrentearpmat
- Deficiencies, Factor 5
- Deficiencies, Factor Five
- Deficiencies, Factor V
- Deficiencies, Labile Factor
- Deficiency, Factor 5
- Deficiency, Factor Five
- Deficiency, Factor V
- Deficiency, Labile Factor
- Disease, Owren
- Disease, Owren's
- Factor 5 Deficiencies
- Factor 5 Deficiency
- Factor Five Deficiencies
- Factor Five Deficiency
- Factor V Deficiencies
- Labile Factor Deficiencies
- Labile Factor Deficiency
- Owren Disease
- Owren Parahemophilia
- Owren's Disease
- Owrens Disease
- Parahemophilia
- Parahemophilia, Owren
- Parahemophilias
Muituimerkejupmi
- a blood coag disord
Fuomášahttin
- A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed)
Fuomášahttin rievdadanhistorjjás
- 73(64); was see under HYPOPROTHROMBINEMIAS 1963-72
Eará gielain
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Finnish
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faktori V:n puute
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faktori V:n puutos
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faktorin V puute
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faktorin V puutos
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FV-puute
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FV-puutos
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hyytymistekijä V:n puute
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hyytymistekijän V puute
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hyytymistekijän V puutos
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proakseleriinin puute
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proakseleriinin puutos
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proakseleriinipuute
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proakseleriinipuutos
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tekijä V:n puute
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tekijä V:n puutos
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tekijän V puute
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tekijän V puutos
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Swedish
URI
http://www.yso.fi/onto/mesh/D005166
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