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| Term | autosomal hemophilia A | ID (Ontology) | DOID:0111823 (Human Disease) |
| Definition | A hemophilia characterized by autosomal inheritance of a Factor VIII deficiency. | ||
| Also Known As | "autosomal Factor VIII deficiency" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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monogenic disease |__autosomal genetic disease__ blood coagulation disease | |__hemophilia_________________| autosomal hemophilia A |
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| Is a |
autosomal genetic disease hemophilia |
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| MIM:134500 | |||