pyruvate kinase deficiency (Q3043149)
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congenital nonspherocytic hemolytic anemia that has material basis in homozygous or compound heterozygous mutation in the PKLR gene on chromosome 1q22
- pyruvate kinase deficiency of red cells
- hemolytic anemia due to red cell pyruvate kinase deficiency
- PK deficiency
- pyruvate kinase deficiency of erythrocyte
- Pyruvate kinase deficiency of erythrocytes
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English | pyruvate kinase deficiency |
congenital nonspherocytic hemolytic anemia that has material basis in homozygous or compound heterozygous mutation in the PKLR gene on chromosome 1q22 |
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C99037
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Sitelinks
Wikipedia(6 entries)
- arwiki نقص البيروفات كايناز
- dewiki Pyruvatkinasemangel
- enwiki Pyruvate kinase deficiency
- frwiki Déficit en pyruvate kinase
- itwiki Deficit di piruvato chinasi
- plwiki Niedobór kinazy pirogronianowej