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Cnossen, Marjon

About me

Name: Marjon

Surname: Cnossen

Academic title: MD PhD

Link to personal website:

https://www.erasmusmc.nl/nl-nl/sophia/patientenzorg/zorgverleners/cnossen-marjon


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  • Prevention and genetic counseling
  • Diagnostics
  • Treatment and care

Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):

Molecular diagnosis, HSCT, etc.

Diseases:

Tumor of hematopoietic and lymphoid tissues Bloom syndrome Deafness-lymphedema-leukemia syndrome Mastocytosis Systemic mastocytosis Indolent systemic mastocytosis Smouldering systemic mastocytosis Isolated bone marrow mastocytosis Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease Aggressive systemic mastocytosis Lymphoadenopathic mastocytosis with eosinophilia Mast cell leukemia Classic mast cell leukemia Aleukemic mast cell leukemia Cutaneous mastocytosis Cutaneous mastocytoma Diffuse cutaneous mastocytosis Bullous diffuse cutaneous mastocytosis Pseudoxanthomatous diffuse cutaneous mastocytosis Maculopapular cutaneous mastocytosis Telangiectasia macularis eruptiva perstans Typical urticaria pigmentosa Plaque-form urticaria pigmentosa Nodular urticaria pigmentosa Mast cell sarcoma Extracutaneous mastocytoma Myeloid hemopathy Acute myeloid leukemia Acute myeloid leukemia with multilineage dysplasia Therapy related acute myeloid leukemia and myelodysplastic syndrome Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Acute myeloid leukemia and myelodysplastic syndromes related to radiation Acute leukemia of ambiguous lineage Acute undifferentiated leukemia Bilineal acute leukemia Acute biphenotypic leukemia Acute myeloid leukemia with recurrent genetic anomaly Acute promyelocytic leukemia Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Acute myeloid leukemia with 11q23 abnormalities Acute myeloid leukemia with t(8;21)(q22;q22) translocation Acute myeloid leukemia with CEBPA somatic mutations Acute myeloid leukemia with t(8;16)(p11;p13) translocation Acute myeloid leukemia with t(6;9)(p23;q34) Acute myeloid leukemia with t(9;11)(p22;q23) Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2) Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) Acute myeloid leukemia with NPM1 somatic mutations Unclassified acute myeloid leukemia Acute erythroid leukemia Acute megakaryoblastic leukemia Acute megakaryoblastic leukemia in Down syndrome Acute megakaryoblastic leukemia without Down syndrome Acute panmyelosis with myelofibrosis Acute basophilic leukemia Myeloid sarcoma Acute myeloid leukemia with minimal differentiation Acute myeloblastic leukemia without maturation Acute myeloblastic leukemia with maturation Acute myelomonocytic leukemia Acute monoblastic leukemia Inherited acute myeloid leukemia Inherited acute myeloid leukemia with presdisposing GAT2 mutation Inherited acute myeloid leukemia with presdisposing RUNX1 mutation Inherited acute myeloid leukemia with presdisposing DDX41 mutation Myelodysplastic syndrome Acquired idiopathic sideroblastic anemia Refractory cytopenia with multilineage dysplasia Refractory anemia Unclassified myelodysplastic syndrome Aregenerative anemia Refractory anemia with excess blasts Refractory anemia with excess blasts type 1 Refractory anemia with excess blasts type 2 Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Refractory anemia with excess blasts in transformation Myeloproliferative neoplasm Essential thrombocythemia Chronic myeloid leukemia Primary myelofibrosis Polycythemia vera Chronic neutrophilic leukemia Chronic myeloproliferative disease, unclassifiable Chronic eosinophilic leukemia Hypereosinophilic syndrome Idiopathic hypereosinophilic syndrome Primary hypereosinophilic syndrome Secondary hypereosinophilic syndrome Lymphocytic hypereosinophilic syndrome Transient myeloproliferative syndrome Hereditary thrombocytopenia with early-onset myelofibrosis Myelodysplastic/myeloproliferative disease Juvenile myelomonocytic leukemia Chronic myelomonocytic leukemia Atypical chronic myeloid leukemia Unclassified myelodysplastic/myeloproliferative disease Myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1 Myeloid neoplasm associated with PDGFRA rearrangement Myeloid neoplasm associated with PDGFRB rearrangement Myeloid neoplasm associated with FGFR1 rearrangement Lymphoid hemopathy Autoimmune lymphoproliferative syndrome Plasma cell tumor POEMS syndrome Multiple myeloma AL amyloidosis Primary systemic amyloidosis Primary localized amyloidosis Plasmacytoma Primary plasmacytoma of the bone Extramedullary soft tissue plasmacytoma Non-amyloid monoclonal immunoglobulin deposition disease Heavy chain deposition disease Light and heavy chain deposition disease Light chain deposition disease Heavy chain disease Mu-heavy chain disease Alpha-heavy chain disease Gamma-heavy chain disease Plasma cell leukemia Immunodeficiency-associated lymphoproliferative disease Post-transplant lymphoproliferative disease Methotrexate-associated lymphoproliferative disorders Lymphoproliferative disease associated with primary immune disease Lymphoma Non-Hodgkin lymphoma Acute lymphoblastic leukemia Precursor B-cell acute lymphoblastic leukemia Precursor T-cell acute lymphoblastic leukemia Mature B-cell acute lymphoblastic leukemia B-cell non-Hodgkin lymphoma Indolent B-cell non-Hodgkin lymphoma Follicular lymphoma Waldenström macroglobulinemia Hairy cell leukemia B-cell chronic lymphocytic leukemia Indolent primary cutaneous B-cell lymphoma Primary cutaneous marginal zone B-cell lymphoma Primary cutaneous follicle center lymphoma Hairy cell leukemia variant Marginal zone lymphoma MALT lymphoma Splenic marginal zone lymphoma Nodal marginal zone B-cell lymphoma Splenic diffuse red pulp small B-cell lymphoma Lymphoplasmacytic lymphoma without IgM production Aggressive B-cell non-Hodgkin lymphoma Burkitt lymphoma Diffuse large B-cell lymphoma Lymphomatoid granulomatosis Primary mediastinal large B-cell lymphoma Intravascular large B-cell lymphoma Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly Diffuse large B-cell lymphoma of the central nervous system T-cell/histiocyte rich large B cell lymphoma Diffuse large B-cell lymphoma with chronic inflammation ALK-positive large B-cell lymphoma Primary effusion lymphoma Mantle cell lymphoma B-cell prolymphocytic leukemia Aggressive primary cutaneous B-cell lymphoma Primary cutaneous diffuse large B-cell lymphoma, leg type Plasmablastic lymphoma T-cell non-Hodgkin lymphoma CD4+/CD56+ hematodermic neoplasm T-cell prolymphocytic leukemia T-cell large granular lymphocyte leukemia Aggressive NK-cell leukemia Adult T-cell leukemia/lymphoma Extranodal nasal NK/T cell lymphoma Enteropathy-associated T-cell lymphoma Hepatosplenic T-cell lymphoma Angioimmunoblastic T-cell lymphoma Anaplastic large cell lymphoma ALK-positive anaplastic large cell lymphoma ALK-negative anaplastic large cell lymphoma Primary cutaneous T-cell lymphoma Indolent primary cutaneous T-cell lymphoma Primary cutaneous CD30+ T-cell lymphoproliferative disease Lymphomatoid papulosis Primary cutaneous anaplastic large cell lymphoma Subcutaneous panniculitis-like T-cell lymphoma Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Mycosis fungoides and variants Classic mycosis fungoides Granulomatous slack skin Folliculotropic mycosis fungoides Localized pagetoid reticulosis Aggressive primary cutaneous T-cell lymphoma Sézary syndrome Primary cutaneous peripheral T-cell lymphoma not otherwise specified Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Primary cutaneous gamma/delta-positive T-cell lymphoma Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood Hydroa vacciniforme-like lymphoma Peripheral T-cell lymphoma NOS Hodgkin lymphoma Classic Hodgkin lymphoma Classic Hodgkin lymphoma, nodular sclerosis type Classic Hodgkin lymphoma, mixed cellularity type Classic Hodgkin lymphoma, lymphocyte-rich type Classic Hodgkin lymphoma, lymphocyte-depleted type Nodular lymphocyte predominant Hodgkin lymphoma Composite lymphoma Primary organ-specific lymphoma Primary pulmonary lymphoma Primary cutaneous lymphoma Primary cutaneous B-cell lymphoma Primary central nervous system lymphoma Thyroid lymphoma Primary oculocerebral lymphoma Primary intraocular lymphoma Primary bone lymphoma Primary lymphoma of the conjunctiva RAS-associated autoimmune leukoproliferative disease Persistent polyclonal B-cell lymphocytosis Castleman disease Pediatric Castleman disease Localized Castleman disease Multicentric Castleman disease Polycythemia Primary familial polycythemia Secondary polycythemia Congenital secondary polycythemia Chuvash erythrocytosis Autosomal recessive secondary polycythemia not associated with VHL gene Autosomal dominant secondary polycythemia Acquired secondary polycythemia Gaisböck syndrome Rare coagulation disorder Rare thrombotic disease of hematologic origin Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to a constitutional coagulation factors defect Congenital factor XII deficiency Familial thrombomodulin anomalies Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Rare hereditary thrombophilia Hereditary thrombophilia due to congenital protein S deficiency Hereditary thrombophilia due to congenital protein C deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Rare thrombotic disorder due to an acquired coagulation factors defect Catastrophic antiphospholipid syndrome Heparin-induced thrombocytopenia Protein S acquired deficiency Acquired purpura fulminans Simple cryoglobulinemia Rare thrombotic disorder due to a platelet anomaly Thrombotic thrombocytopenic purpura Congenital thrombotic thrombocytopenic purpura Acquired thrombotic thrombocytopenic purpura Rare thrombotic disorder due to a constitutional platelet anomaly Familial thrombocytosis Hereditary thrombocytosis with transverse limb defect Rare thrombotic disorder due to an acquired platelet anomaly Rare hemorrhagic disorder Rare hemorrhagic disorder due to a coagulation factors defect Rare hemorrhagic disorder due to a constitutional coagulation factors defect Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Hemophilia Hemophilia A Severe hemophilia A Moderately severe hemophilia A Mild hemophilia A Symptomatic form of hemophilia A in female carriers Hemophilia B Severe hemophilia B Moderately severe hemophilia B Mild hemophilia B Symptomatic form of hemophilia B in female carriers Congenital factor V deficiency Congenital fibrinogen deficiency Familial afibrinogenemia Familial dysfibrinogenemia Familial hypofibrinogenemia Familial hypodysfibrinogenemia Congenital alpha2-antiplasmin deficiency Congenital factor XIII deficiency Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 2A Von Willebrand disease type 2B Von Willebrand disease type 2M Von Willebrand disease type 2N Von Willebrand disease type 3 Congenital factor XI deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital high-molecular-weight kininogen deficiency Congenital prekallikrein deficiency Combined deficiency of factor V and factor VIII Congenital vitamin K-dependent coagulation factors deficiency Congenital factor VII deficiency Congenital factor II deficiency Congenital factor X deficiency Hereditary combined deficiency of vitamin K-dependent clotting factors Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation East Texas bleeding disorder Thrombomodulin-related bleeding disorder Rare hemorrhagic disorder due to an acquired coagulation factor defect Acquired prothrombin deficiency Acquired hemophilia Acquired von Willebrand syndrome Rare hemorrhagic disorder due to a platelet anomaly Rare hemorrhagic disorder due to a constitutional platelet anomaly Rare hemorrhagic disorder due to a constitutional thrombocytopenia Syndromic constitutional thrombocytopenia Stormorken-Sjaastad-Langslet syndrome Thrombocytopenia-absent radius syndrome Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome MYH9-related disease GNE myopathy Jacobsen syndrome Macrothrombocytopenia with mitral valve insufficiency Alpha delta granule deficiency Dense granule disease Wiskott-Aldrich syndrome Chédiak-Higashi syndrome Hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome Hermansky-Pudlak syndrome Hermansky-Pudlak syndrome with neutropenia Hermansky-Pudlak syndrome with pulmonary fibrosis Hermansky-Pudlak syndrome without pulmonary fibrosis Hermansky-Pudlak syndrome type 7 Hermansky-Pudlak syndrome type 8 Hermansky-Pudlak syndrome type 9 Isolated constitutional thrombocytopenia Isolated hereditary giant platelet disorder Severe autosomal recessive macrothrombocytopenia Bernard-Soulier syndrome Thrombocytopenia with congenital dyserythropoietic anemia Autosomal dominant macrothrombocytopenia Alpha granule disease Gray platelet syndrome Quebec platelet disorder Medich giant platelet syndrome White platelet syndrome Paris-Trousseau thrombocytopenia X-linked dyserythropoetic anemia with abnormal platelets and neutropenia Hereditary thrombocytopenia with normal platelets X-linked thrombocytopenia with normal platelets Autosomal thrombocytopenia with normal platelets Congenital amegakaryocytic thrombocytopenia Bleeding diathesis due to thromboxane synthesis deficiency Isolated delta-storage pool disease Autosomal dominant thrombocytopenia with platelet secretion defect Rare hemorrhagic disorder due to a qualitative platelet defect Glanzmann thrombasthenia Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Ehlers-Danlos syndrome, fibronectinemic type Scott syndrome P2Y12 defect Pseudo-von Willebrand disease Bleeding diathesis due to a collagen receptor defect Bleeding diathesis due to glycoprotein VI deficiency Bleeding diathesis due to integrin alpha2-beta1 deficiency Bleeding disorder due to CalDAG-GEFI deficiency Rare hemorrhagic disorder due to an acquired platelet anomaly Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome TAFRO syndrome HELLP syndrome Fetal and neonatal alloimmune thrombocytopenia Autoimmune thrombocytopenia Immune thrombocytopenic purpura Evans syndrome STAT3-related early-onset multisystem autoimmune disease Kasabach-Merritt syndrome Rare anemia Thiamine-responsive megaloblastic anemia syndrome Hemoglobinopathy Hemoglobin E disease Hemoglobin D disease Unstable hemoglobin disease Alpha-thalassemia and related diseases Alpha-thalassemia Hemoglobin H disease Hb Bart's hydrops fetalis Alpha-thalassemia-related diseases Alpha-thalassemia-X-linked intellectual disability syndrome Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Alpha-thalassemia-myelodysplastic syndrome Beta-thalassemia and related diseases Beta-thalassemia Beta-thalassemia major Beta-thalassemia intermedia Dominant beta-thalassemia Beta-thalassemia associated with another hemoglobin anomaly Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Delta-beta-thalassemia Hemoglobin C-beta-thalassemia syndrome Hemoglobin E-beta-thalassemia syndrome Hemoglobin Lepore-beta-thalassemia syndrome Beta-thalassemia with other manifestations Beta-thalassemia-X-linked thrombocytopenia syndrome Sickle cell disease and related diseases Sickle cell anemia Sickle cell disease associated with an other hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Hemoglobinopathy Toms River Hereditary methemoglobinemia Hemoglobin C disease Hemoglobin M disease Acquired methemoglobinemia Rare hemolytic anemia Rare constitutional hemolytic anemia Atypical hemolytic-uremic syndrome Atypical hemolytic-uremic syndrome with DGKE deficiency Atypical hemolytic-uremic syndrome with C3 anomaly Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly Atypical hemolytic-uremic syndrome with B factor anomaly Atypical hemolytic-uremic syndrome with H factor anomaly Atypical hemolytic-uremic syndrome with I factor anomaly Atypical hemolytic-uremic syndrome with anti-factor H antibodies Atypical hemolytic-uremic syndrome with thrombomodulin anomaly Rare constitutional hemolytic anemia due to a red cell membrane anomaly Hereditary spherocytosis Hereditary elliptocytosis Distal renal tubular acidosis with anemia Hereditary stomatocytosis Overhydrated hereditary stomatocytosis Dehydrated hereditary stomatocytosis Rh deficiency syndrome Familial pseudohyperkalemia Southeast Asian ovalocytosis Hereditary cryohydrocytosis with reduced stomatin Hereditary cryohydrocytosis with normal stomatin Constitutional hemolytic anemia due to acanthocytosis Abetalipoproteinemia McLeod neuroacanthocytosis syndrome Primary CD59 deficiency Rare constitutional hemolytic anemia due to an enzyme disorder Congenital erythropoietic porphyria Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies Glutathione synthetase deficiency Glutathione synthetase deficiency with 5-oxoprolinuria Glutathione synthetase deficiency without 5-oxoprolinuria Gamma-glutamylcysteine synthetase deficiency Hemolytic anemia due to glutathione reductase deficiency 6-phosphogluconate dehydrogenase deficiency Hemolytic anemia due to a disorder of glycolytic enzymes Glycogen storage disease due to muscle phosphofructokinase deficiency Triose phosphate-isomerase deficiency Glycogen storage disease due to aldolase A deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Hemolytic anemia due to red cell pyruvate kinase deficiency Hemolytic anemia due to glucophosphate isomerase deficiency Hemolytic anemia due to diphosphoglycerate mutase deficiency Non-spherocytic hemolytic anemia due to hexokinase deficiency Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Class I glucose-6-phosphate dehydrogenase deficiency Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Hemolytic anemia due to adenylate kinase deficiency Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Heinz body anemia Rare acquired hemolytic anemia Paroxysmal nocturnal hemoglobinuria Typical hemolytic-uremic syndrome Aplastic anemia Rare constitutional aplastic anemia Blackfan-Diamond anemia Dyskeratosis congenita Fanconi anemia Revesz syndrome Hoyeraal-Hreidarsson syndrome WT limb-blood syndrome Shwachman-Diamond syndrome Autosomal dominant aplasia and myelodysplasia Hereditary isolated aplastic anemia Pancytopenia-developmental delay syndrome Rare acquired aplastic anemia Idiopathic aplastic anemia Red cell aplasia Transient erythroblastopenia of childhood Adult pure red cell aplasia Monocytopenia with susceptibility to infections Rare deficiency anemia Constitutional deficiency anemia Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder Methylmalonic acidemia with homocystinuria Methylmalonic acidemia with homocystinuria, type cblC Methylmalonic acidemia with homocystinuria, type cblD Methylmalonic acidemia with homocystinuria type cblF Methylmalonic acidemia with homocystinuria, type cblJ Methylmalonic acidemia with homocystinuria, type cblX Transcobalamin deficiency Congenital intrinsic factor deficiency Homocystinuria without methylmalonic aciduria Methylcobalamin deficiency type cblE Methylcobalamin deficiency type cblG Methylcobalamin deficiency type cblDv1 Gräsbeck-Imerslund disease Constitutional megaloblastic anemia due to folate metabolism disorder Formiminoglutamic aciduria Hereditary folate malabsorption Constitutional megaloblastic anemia with severe neurologic disease Vitamin B12- and folate-independent constitutional megaloblastic anemia Hereditary orotic aciduria Hypoxanthine-guanine phosphoribosyltransferase deficiency Lesch-Nyhan syndrome Hypoxanthine guanine phosphoribosyltransferase partial deficiency Constitutional dyserythropoietic anemia Congenital dyserythropoietic anemia Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type II Congenital dyserythropoietic anemia type IV Majeed syndrome Pancreatic insufficiency-anemia-hyperostosis syndrome

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