Orphanet classification of rare genetic diseases
- Rare genetic disease
ORPHA:98053 -
Rare genetic hematologic disease
ORPHA:158300 -
Congenital analbuminemia ORPHA:86816
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Genetic polycythemia ORPHA:250165
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L-ferritin deficiency ORPHA:440731
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Paroxysmal nocturnal hemoglobinuria ORPHA:447
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Rare constitutional anemia ORPHA:183651
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Rare genetic coagulation disorder ORPHA:183654
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