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| Term | congenital amegakaryocytic thrombocytopenia | ID (Ontology) | DOID:0090118 (Human Disease) |
| Definition | A thrombocytopenia that is characterized by a severe reduction in megakaryocyte and platelet numbers. | ||
| Also Known As | "CAMT" ; "congenital amegakaryocytic thrombocytopenic purpura" | ||
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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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autosomal genetic disease |__autosomal recessive disease__ blood platelet disease | |__thrombocytopenia_____________| disease | |__physical disorder____________| congenital amegakaryocytic thrombocytopenia |__congenital amegakaryocytic thrombocytopenia 1 |__congenital amegakaryocytic thrombocytopenia 2 |
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| Is a |
autosomal recessive disease physical disorder thrombocytopenia |
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External Crossreferences & Linkouts
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GARD:640 MESH:C535982 NCI:C115207 ORDO:3319 SNOMEDCT_US_2023_03_01:716336002 UMLS_CUI:C1327915 |
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