All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01754 ECYT8 erythrocytosis, familial, type 8 (ECYT8, bisphosphoglycerate mutase deficiency) 222800 AR 2 2 BPGM - -
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