| Descriptor English: | Factor V Deficiency | ||||||
| Descriptor Spanish: |
Deficiencia del Factor V
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| Descriptor Portuguese: | Deficiência do Fator V | ||||||
| Descriptor French: | Déficit en facteur V | ||||||
| Entry term(s): |
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 |
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| Tree number(s): |
C15.378.100.100.300 C15.378.100.141.300 C15.378.463.300 C16.320.099.300 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005166 | ||||||
| Scope note: | 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) |
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| Annotation: | a blood coag disord |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 73; was see under HYPOPROTHROMBINEMIAS 1963-72 |
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| Online Note: | use HYPOPROTHROMBINEMIAS to search FACTOR V DEFICIENCY 1966-72 |
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| History Note: | 73(64); was see under HYPOPROTHROMBINEMIAS 1963-72 |
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| Entry Version: | FACTOR V DEFIC |
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| DeCS ID: | 5266 | ||||||
| Unique ID: | D005166 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1973/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2017/05/02 |
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Factor V Deficiency
- Preferred
| Concept UI |
M0008143 |
| Scope note | 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) |
| Preferred term | Factor V Deficiency |
| Entry term(s) |
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 |
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