Diagnosing immune-related disorders precisely can provide life-changing treatment and options to better manage disease. By leveraging our robust and comprehensive rare disease-centric Bio/Databank, we carefully curate and document all variants that clinically correlate to symptoms – providing a comprehensive diagnosis of immune-related diseases.

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Bone Marrow Failure/Anemia Panel

Our bone marrow failure/anemia panel is intended for patients with abnormalities in more than two blood cell types (red blood cell, white blood cell, and platelets) who present symptoms of lethargy, recurrent infections, excessive bleeding, abnormal pigmentation, enlarged spleen, and malignancies. Some specific disorders detected with this panel are hemophagocytic lymphohistiocytosis, Seckel syndrome, thrombocytopenia, Fanconi anemia, dyskeratosis congenita, Shwachman Diamond syndrome as well as other types of anemias, such as thalassemia alpha and beta, sickle cell disease, spherocytosis, megaloblastic anemia, congenital sideroblastic, and dyserythropoietic anemia.

No. of genes: 211
TAT: 25 days
Coverage: ≥99.0% ≥20x
Details: CNV analysis included

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  • Bone marrow failure syndrome
  • Congenital dyserythropoietic anemia
  • Congenital sideroblastic anemia
  • Diamond-Blackfan anemia
  • Fanconi anemia
  • Hemophagocytic lymphohistiocytosis
  • Hereditary spherocytosis
  • Megaloblastic anemia
  • Seckel syndrome
  • Thrombocytopenia


CentoImmuno is our solution for immunodeficiency and severe combined immunodeficiency (SCID) disorders. Our panel includes genes targeting severe combined immunodeficiency, congenital neutropenia, primary antibody deficiency, common variable immune deficiency, chronic granulomatous disease, autoimmune lymphoproliferative, and agammaglobulinemia.

No. of genes: 326
TAT: 25 days
Coverage: ≥99.0% ≥20x
Details: CNV analysis included

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  • Agammaglobulinemia
  • Autoimmune lymphoproliferative syndrome
  • B-cell-negative severe combined immunodeficiency
  • B-cell-positive severe combined immunodeficiency
  • Chronic granulomatous disease
  • Common variable immune deficiency
  • Congenital afibrinogenemia
  • Congenital neutropenia syndromes
  • Hermasky-Pudlak syndrome
  • Mendelian susceptibility to mycobacterial diseases
  • Periodic fever syndrome
  • Primary antibody deficiency
  • Primary ciliary dyskinesia
  • Primary immunodeficiencies (PID)
  • Severe combined immunodeficiency

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CentoPortal® is a user-friendly, online, web-based ordering portal designed to assist you at every step of processing your patients' samples.

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