Name | Factor XI Deficiency |
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Synonyms | Deficiencies, Factor 11 | Deficiencies, Factor Eleven | Deficiencies, Factor XI | Deficiency, Factor 11 | Deficiency, Factor Eleven | Deficiency, Factor XI | F11 DEFICIENCY | Factor 11 Deficiencies | Factor 11 Deficiency | Factor Eleven Deficiencies | Factor Eleven Deficiency | Factor XI Deficiencies | Hemophilia C | Plasma Thromboplastin Antecedent Deficiency | PTA DEFICIENCY | Rosenthal's Syndrome | Rosenthals Syndrome | Rosenthal's Syndromes | Rosenthal Syndrome | Rosenthal Syndromes | Syndrome, Rosenthal | Syndrome, Rosenthal's |
Definition | A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia. |
Categories | Blood disease | Genetic disease (inborn) |
MeSH® ID | D005173 |
OMIM® ID | 612416 |
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Diseases
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Hemic and Lymphatic Diseases
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Diseases
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Hemic and Lymphatic Diseases
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Diseases
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Hemic and Lymphatic Diseases
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Diseases
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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