All diseases

OMIM ID
240300
OMIM term:
AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I; APS1
Alternative terms:
APS I
AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY; APECED
AUTOIMMUNE POLYGLANDULAR SYNDROME, TYPE I
POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE I
PGA I
HYPOADRENOCORTICISM WITH HYPOPARATHYROIDISM AND SUPERFICIAL MONILIASIS POLYGLANDULAR DEFICIENCY SYNDROME, PERSIAN-JEWISH TYPE, INCLUDED
AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, AUTOSOMAL DOMINANT, INCLUDED
AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA, INCLUDED
(∗) Location:
21q22.3  
(†) Associated OMIM genes:
AIRE  
(‡) Associated MGI genes:
Aire  

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* quick link - http://q.sanger.ac.uk/0pn61q01