All diseases

OMIM ID
242860
OMIM term:
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1; ICF1
Alternative terms:
IMMUNE DEFICIENCY, VARIABLE, WITH CENTROMERIC INSTABILITY OF CHROMOSOMES 1, 9, AND 16
CENTROMERIC INSTABILITY, IMMUNODEFICIENCY SYNDROME; CIID
IMMUNODEFICIENCY SYNDROME, VARIABLE
(∗) Location:
20q11.21  
(†) Associated OMIM genes:
DNMT3B  
(‡) Associated MGI genes:
Dnmt3a   Dnmt3b  

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