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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 polycythemia
Erythrocytosis, familial, 6
rare
Identifiers
MONDO:0054801
OMIM:617980
Causal genes
HBB
Part of
Familial polycythemia
Also known as
ECYT6 · erythrocytosis 6
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