Congenital hematological disorder
MONDO:0009332A disorder of the blood that is present at birth.
Also known as: congenital haematological system disease, congenital hematological disorder, congenital hematological system disease
101 clinical trials for this condition and its sub-types, 1 tagged with Congenital hematological disorder itself.
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Sub-types of Congenital hematological disorder
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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
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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
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Congenital vitamin K-dependent coagulation factors deficiency 0 trials · 4 incl. sub-types
5 sub-types
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GNE myopathy 3 trials
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Congenital factor XII deficiency 1 trial
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Congenital agammaglobulinemia 0 trials
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Congenital analbuminemia 0 trials
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Congenital factor XI deficiency 0 trials
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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
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Congenital secondary polycythemia 0 trials
2 sub-types
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2 sub-types
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Sulfhemoglobinemia, congenital 0 trials
Most studied deeper sub-types
Pyruvate kinase deficiency of red cells
(10)
Fanconi anemia complementation group D1
(6)
Fanconi anemia complementation group A
(4)
Fanconi anemia complementation group E
(4)
Kostmann syndrome
(3)
Fanconi anemia complementation group N
(2)
Fanconi anemia, complementation group S
(2)
Anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane
(1)
Anemia, nonspherocytic hemolytic, due to G6PD deficiency
(1)
Hemolytic anemia due to adenylate kinase deficiency
(1)
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
(1)
Neutropenia, severe congenital, 8, autosomal dominant
(1)
Anemia, congenital dyserythropoietic, type 1a
(0)
Anemia, nonspherocytic hemolytic
(0)
Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism
(0)
Autosomal dominant severe congenital neutropenia
(0)
Autosomal recessive severe congenital neutropenia
(0)
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
(0)
Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
(0)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
(0)