Deutsch
Clinical AreaHematology
Associated diseases
- Adenosine deaminase 2 deficiency, differential diagnosis
- Autoimmune hemolytic anemia; differential diagnosis
- Barth syndrome, differential diagnosis
- Bernard-Soulier syndrome, differential diagnosis
- Beta globinopathies
- Bloom syndrome, differential diagnosis
- Bone marrow dysfunction, hereditary; differential diagnosis
- C1Q deficiency
- Chediak-Higashi syndrome
- Coagulation disorders, coagulopathies; differential diagnosis
- Coagulation disorders, differential diagnosis
- Diamond-Blackfan anemia, aplastic; differential diagnosis
- Erythrocyte membrane defects, differential diagnosis
- Erythrocytosis, familial hereditary; differential diagnosis
- Factor II deficiency, Prothrombin mutation; Thrombophilia
- Factor V + factor VIII deficiency, combined
- Fanconi anemia, differential diagnosis
- Haematological malignancies, germline mutations; differential diagnosis
- Haemolytic anaemia, non-sphaerocytic
- Hemostasis disorders, inherited; differential diagnosis
- Hermansky-Pudlak syndrome, differential diagnosis
- Hyper-IgM syndrome, XL; differential diagnosis
- Iron-refractory iron deficiency anemia, IRIDA; differential diagnosis
- Juvenile hemochromatosis [type 2], differential diagnosis
- Leukaemia, acute lymphoblastic, hereditary; susceptibility
- Leukaemia, chronic myeloid; hereditary
- Leukaemia, chronic myelomonocytic, hereditary; differential diagnosis
- Leukemia, acute myeloic; hereditary; differential diagnosis
- Leukemia, chronic neutrophilic, hereditary: differential diagnosis
- Lupus [erythematosus], "monogenic"; differential diagnosis
- Lymphohistiozytosis, familial hemophagocytic; differential diagnosis
- Lymphoid malignancy, predisposition
- Lymphoma, follicular; prognosis
- Lymphoproliferative disease, X chromosomal; differential diagnosis
- Macrothrombocytopenias, differential diagnosis
- Mastocytosis, differential diagnosis
- McLeod neuroacanthocytosis syndrome; differential diagnosis
- MIRAGE syndrome, differential diagnosis
- Monosomy 7 predisposition syndromes, differential diagnosis
- Morbus Waldenstrom, mutations + predisposition
- Multiple myeloma, susceptibility
- Myelodysplastic syndromes, hereditary; differential diagnosis
- Myelofibrosis, primary; hereditary
- Myeloproliferative neoplasia - genetic predisposition
- Neutropenia, congenital; differential diagnosis
- Neutropenia, cyclic; differential diagnosis
- Paroxysmal nocturnal haemoglobinuria 2
- Plasminogen activator inhibitor 1 deficiency, differential diagnosis
- Polycythaemia vera, familial hereditary; differential diagnosis
- Polycythemia/paraganglioma/pheochromocytoma, differential diagnosis
- Porphyria, differential diagnosis
- Porphyria, erythropoetic 1
- Protein C deficiency; thrombophilia
- Protein S deficiency; thrombophilia
- Rendu-Osler-Weber disease, differential diagnosis
- Sebastian syndrome, differential diagnosis
- Seltene hämatologische neoplastische Syndrome; hereditär
- Sickle cell disease
- Sphaerocytosis, hereditary; spherocytosis
- Thalassaemia alpha
- Thalassaemia beta
- Thalassemia alpha + thalassemia beta
- Thrombocyte function disturbances/thrombocytopathies
- Thrombocytopenias + thrombocytopathies, hereditary; differential diagnosis
- VEXAS-Syndrom
Notes on the clinical area
Here you will find the disease-related gene panels available for the clinical area specified above.
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