All diseases

OMIM ID
133100
OMIM term:
ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1
Alternative terms:
POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP
ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN
(∗) Location:
12q24.12   19p13.2  
(†) Associated OMIM genes:
EPOR   SH2B3  
(‡) Associated MGI genes:
Epor  

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