All diseases

OMIM ID
182900
OMIM term:
SPHEROCYTOSIS, TYPE 1; SPH1
Alternative terms:
SPHEROCYTOSIS, HEREDITARY, 1; HS1
SPH; HS
(∗) Location:
8p11.21  
(†) Associated OMIM genes:
ANK1  
(‡) Associated MGI genes:
Add2   Ank1   Epb4.2   Spna1  

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