Congenital hematological disorder

Part of

Sub-types of Congenital hematological disorder

• Congenital anemia 0 trials · 58 incl. sub-types
  8 sub-types

  • Fanconi anemia 29 trials · 42 incl. sub-types Sub-types →
  • Congenital nonspherocytic hemolytic anemia 1 trial · 12 incl. sub-types Sub-types →
  • Myopathy, lactic acidosis, and sideroblastic anemia 3 trials Sub-types →
  • Congenital dyserythropoietic anemia type 1 1 trial Sub-types →
  • Congenital dyserythropoietic anemia type 2 1 trial
  • Congenital dyserythropoietic anemia type 3 0 trials
  • Congenital dyserythropoietic anemia type 4 0 trials
  • Severe congenital hypochromic anemia with ringed sideroblasts 0 trials
• Constitutional neutropenia 2 trials · 28 incl. sub-types
  13 sub-types

  • Chediak-Higashi syndrome 9 trials
  • Severe congenital neutropenia 5 trials · 8 incl. sub-types Sub-types →
  • Barth syndrome 5 trials
  • WHIM syndrome 1 4 trials
  • Glycogen storage disease Ib 3 trials
  • Cohen syndrome 1 trial
  • Griscelli syndrome type 2 1 trial
  • Cyclic hematopoiesis 1 trial
  • Hermansky-Pudlak syndrome 2 0 trials
  • Lichtenstein syndrome 0 trials
  • Neutropenia-monocytopenia-deafness syndrome 0 trials
  • Poikiloderma with neutropenia 0 trials
  • Primary immunodeficiency syndrome due to p14 deficiency 0 trials
• Congenital thrombotic thrombocytopenic purpura 5 trials
• Congenital vitamin K-dependent coagulation factors deficiency 0 trials · 4 incl. sub-types
  5 sub-types

  • Congenital factor VII deficiency 3 trials
  • Vitamin K-dependent clotting factors, combined deficiency of, type 1 1 trial
  • Congenital factor X deficiency 0 trials
  • Congenital prothrombin deficiency 0 trials
  • Vitamin K-dependent clotting factors, combined deficiency of, type 2 0 trials
• GNE myopathy 3 trials
• Congenital amegakaryocytic thrombocytopenia 1 3 trials
• Leukocyte adhesion deficiency type II 2 trials
• Congenital factor XII deficiency 1 trial
• Congenital plasminogen activator inhibitor type 1 deficiency 1 trial
• Thrombocytopenia-absent radius syndrome 1 trial
• Congenital agammaglobulinemia 0 trials
  2 sub-types

  • Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome 0 trials
  • Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia 0 trials
• Congenital analbuminemia 0 trials
• Congenital factor XI deficiency 0 trials
• Congenital factor XIII deficiency 0 trials
  2 sub-types

  • Factor XIII, A subunit, deficiency of 0 trials
  • Factor XIII, b subunit, deficiency of 0 trials
• Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome 0 trials
• Congenital secondary polycythemia 0 trials
  2 sub-types

  • Chuvash polycythemia 0 trials
  • Autosomal recessive secondary polycythemia not associated with VHL gene 0 trials
• Hereditary thrombocytosis with transverse limb defect 0 trials
• Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 0 trials
• Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome 0 trials
• Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome 0 trials
  2 sub-types

  • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 0 trials
  • Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0 trials
• Sulfhemoglobinemia, congenital 0 trials