All diseases

OMIM ID
251260
OMIM term:
NIJMEGEN BREAKAGE SYNDROME
Alternative terms:
NBS
ATAXIA-TELANGIECTASIA VARIANT V1; AT-V1
MICROCEPHALY WITH NORMAL INTELLIGENCE, IMMUNODEFICIENCY, AND LYMPHORETICULAR MALIGNANCIES
SEEMANOVA SYNDROME II
NONSYNDROMAL MICROCEPHALY, AUTOSOMAL RECESSIVE, WITH NORMAL INTELLIGENCE
IMMUNODEFICIENCY, MICROCEPHALY, AND CHROMOSOMAL INSTABILITY BERLIN BREAKAGE SYNDROME, INCLUDED; BBS, INCLUDED
ATAXIA-TELANGIECTASIA VARIANT V2, INCLUDED; AT-V2, INCLUDED
(∗) Location:
8q21.3  
(†) Associated OMIM genes:
NBN  
(‡) Associated MGI genes:
Nbn  

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