All diseases

OMIM ID
129200
OMIM term:
ADERMATOGLYPHIA WITH CONGENITAL FACIAL MILIA AND ACRAL BLISTERS, DIGITAL CONTRACTURES, AND NAIL ABNORMALITIES
Alternative terms:
ECTODERMAL DYSPLASIA, ABSENT DERMATOGLYPHIC PATTERN, CHANGES IN NAILS, AND SIMIAN CREASE
BASAN SYNDROME
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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