Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII

SNOMEDCT-BE (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may / 733028000

SNOMEDCT-BE (disorder) / 733028000

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

antihaemophilic factor A | clotting agent for haemophiliacs | factor 8 | factor VIII

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

facteur antihémophilique A | facteur VIII

IATE - Health

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

facteur antihémophile A | facteur VIII

IATE - Health

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

recombinant factor VIII | rF VIII C [Abbr.]

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

facteur VIII recombinant | rF VIII C [Abbr.]

IATE - Health

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in t

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

déficit combiné en facteurs V et VIII

SNOMEDCT-BE (chromosome 18; q21) or in t / 715559004

SNOMEDCT-BE (disorder) / 715559004

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Von Willebrand factor | factor VIII:R

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

facteur Willebrand | facteur VIII : R Ag | antigène Willebrand | cofacteur de la ristocétine

médecine > hématologie et sérologie | médecine > transfusion

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

Deficiency factor VIII (with functional defect) Haemophilia:NOS | A | classical

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Carence en facteur VIII (avec anomalie fonctionnelle) Hémophilie:SAI | A | classique

WORLD HEALTH ORGANIZATION ICD-10: D66

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Hereditary factor VIII deficiency

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Carence héréditaire en facteur VIII

WORLD HEALTH ORGANIZATION ICD-10: D66

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Others have searched : factor viii ag hereditary factor viii deficiency von willebrand factor antihaemophilic factor antihaemophilic globulin antihemophilic factor antihemophilic globulin blood clotting protein classical clotting agent for haemophiliacs factor factor viii rf viii recombinant factor viii

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'factor viii ag'

Date index:2021-01-09 -

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Translation of "factor viii ag " (English → French) :

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