- OMIM ID
-
136500
- OMIM term:
- BRAUER SYNDROME
- Alternative terms:
-
FOCAL FACIAL DERMAL DYSPLASIA, TYPE I
FFDD, TYPE I
HEREDITARY SYMMETRICAL APLASTIC NEVI OF TEMPLES
BITEMPORAL APLASIA CUTIS CONGENITA
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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