Phenotypes for disease #01754 (ECYT8 (erythrocytosis, familial, type 8 (ECYT8, bisphosphoglycerate mutase deficiency)), OMIM:222800)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000188406 Bisphosphoglycerate mutase deficiency - - Familial, autosomal recessive - 42y - - - LOVD 00249441
0000188407 see paper; ..., asymptomatic/plethora congenital erythrocytosis ECYT8 Familial, autosomal recessive - 28y - - - LOVD 00249442
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