All diseases

OMIM ID
601859
OMIM term:
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; ALPS
Alternative terms:
CANALE-SMITH SYNDROME
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL DOMINANT AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IA, INCLUDED; ALPS1A, INCLUDED
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IB, INCLUDED; ALPS1B, INCLUDED
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL RECESSIVE, INCLUDED
(∗) Location:
10q23.31   1q24.3  
(†) Associated OMIM genes:
TNFRSF6   TNFSF6  
(‡) Associated MGI genes:
Fas   Fasl  

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