All diseases

OMIM ID
105600
OMIM term:
ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE III; CDAN3
Alternative terms:
DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE III
CDA III
ANEMIA WITH MULTINUCLEATED ERYTHROBLASTS
ERYTHRORETICULOSIS, HEREDITARY BENIGN
(∗) Location:
15q21  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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