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megaloblastic anemia
(phenotype)
Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
GIF
AMN
CUBN
SLC19A1
SLC19A2
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
vitamin metabolic process
vitamin transport
drug transport
MANALO_HYPOXIA_DN
REACTOME_METABOLISM_OF_VITAMINS_AND_COFACTORS
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Metabolic disease
OMIM - Anemia
OMIM - Congenital disorder
OMIM - Anemias
OMIM - Immunodeficiency disorder
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Literature
Most Relevant Literature
Does early treatment prevent deafness in thiamine-responsive megaloblastic anaemia syndrome?
Megaloblastic anemia--a rare cause.
Thiamine responsive megaloblastic anemia with a novel SLC19A2 mutation presenting with myeloid matur…
A dimorphic blood film as a sign of the onset of iron-deficient erythropoiesis in megaloblastic anem…
Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and…
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Clinical Trials
Most Relevant Clinical Trials
Megadose of Hydroxocobalamin for the Treatment of Pernicious Anemia
A Double-blind Study of KRN321 for the Treatment of Anemia in Cancer Patients
A Dose Finding Study of KRN321(Darbepoetin Alfa) for the Treatment of Anemia in Subjects With Solid …
Trial of Captafer® vs. Oral Iron Sulfate in the Treatment of Iron Deficiency Anemia in Patients With…
Folic Acid Supplementation in Children With Sickle Cell Disease
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