All diseases

OMIM ID
105650
OMIM term:
DIAMOND-BLACKFAN ANEMIA; DBA
Alternative terms:
BLACKFAN-DIAMOND SYNDROME; BDS
ANEMIA, CONGENITAL HYPOPLASTIC, OF BLACKFAN AND DIAMOND
ANEMIA, CONGENITAL ERYTHROID HYPOPLASTIC
RED CELL APLASIA, PURE, HEREDITARY
AREGENERATIVE ANEMIA, CHRONIC CONGENITAL
ERYTHROGENESIS IMPERFECTA
AASE-SMITH SYNDROME II
AASE SYNDROME DIAMOND-BLACKFAN ANEMIA 1, INCLUDED; DBA1, INCLUDED
(∗) Location:
19q13.2  
(†) Associated OMIM genes:
RPS19  
(‡) Associated MGI genes:
Mfsd7b   Rpsa  

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