All diseases

OMIM ID
607271
OMIM term:
CASPASE 8 DEFICIENCY
Alternative terms:
CEDS
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIB; ALPS2B
(∗) Location:
2q33.1  
(†) Associated OMIM genes:
CASP8  
(‡) Associated MGI genes:

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