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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Familial hemolytic anemia
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Congenital dyserythropoietic anemia
Anemia, congenital dyserythropoietic, type IVb
rare
Identifiers
MONDO:0975829
OMIM:620969
Causal genes
KLF1
Part of
Congenital dyserythropoietic anemia
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