All diseases

OMIM ID
603554
OMIM term:
OMENN SYNDROME
Alternative terms:
RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA
SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA
(∗) Location:
10p13   11p12  
(†) Associated OMIM genes:
DCLRE1C   RAG1   RAG2  
(‡) Associated MGI genes:
Rag2  

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