All diseases

OMIM ID
153550
OMIM term:
CHROMOSOME 5q DELETION SYNDROME
Alternative terms:
5q- SYNDROME
MACROCYTIC ANEMIA, REFRACTORY, DUE TO 5q DELETION; MAR MEGAKARYOCYTES, UNILOBULAR NUCLEATED, INCLUDED
(∗) Location:
5q33.1  
(†) Associated OMIM genes:
RPS14  
(‡) Associated MGI genes:
Lmo2  

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