All diseases

OMIM ID
604290
OMIM term:
ACERULOPLASMINEMIA HYPOCERULOPLASMINEMIA, INCLUDED
Alternative terms:
CERULOPLASMIN DEFICIENCY, INCLUDED
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA, INCLUDED
(∗) Location:
3q24-q25  
(†) Associated OMIM genes:
CP  
(‡) Associated MGI genes:
Cp  

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