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Red blood cell disorder
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
HBB
HBA1
SLC4A1
HBA2
BPGM
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
HALLMARK_HEME_METABOLISM
heterocycle metabolic process
organic cyclic compound metabolic process
DIAZ_CHRONIC_MEYLOGENOUS_LEUKEMIA_UP
PUJANA_BRCA1_PCC_NETWORK
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Curated Studies
Most Correlated Studies
Pediatric myelodysplastic syndrome gene expression profiles associated with disease subtype
Gene expression profiles in Diamond-Blackfan anemia patients.
Genome wide expression in ADAMTS13-deficient thrombotic thrombocytopenic purpura TTP
TK6 cells treated with various clastogens, aneugens and formaldehyde
CD71 high c-Kit high pro-erythroblasts with erythroid-specific LSD1 deletion
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Literature
Most Relevant Literature
Red blood cell disorders in recently arrived African immigrants to Gran Canaria, Spain.
Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders…
Reprogramming based gene therapy for inherited red blood cell disorders.
Strides made in red blood cell disorders, but substantial barriers to care remain.
Red blood cell enzyme disorders: an overview.
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Clinical Trials
Most Relevant Clinical Trials
Pathophysiological Explorations of Red Blood Cells
Evaluation of Spectra Optia Red Blood Cell Exchange in Sickle Cell Patients
Transfusion of Biotinylated Red Blood Cells
Electric Polarization of Red Blood Cells : A Cohort Study to Assess the Erythrocytes Membrane Integr…
Study to Evaluate Efficacy and Safety of S303 Treated Red Blood Cells (RBCs)in Subjects With Thalass…
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