Ontologiesccoclasses300653   
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Phosphoglycerate kinase 1 deficiencyImported
http://identifiers.org/omim/300653

(PGK1D) - A condition with a highly variable clinical phenotype that includes hemolytic anemia, rhabdomyolysis, myopathy and neurologic involvement. Patients can express one or more of these manifestations.

Also appears ingexoretorexo
class Information
alternative label

PGK1D

preferred label

Phosphoglycerate kinase 1 deficiency

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Subclass of

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