- OMIM ID
-
302380
- OMIM term:
- CATEL-MANZKE SYNDROME
- Alternative terms:
-
HYPERPHALANGY-CLINODACTYLY OF INDEX FINGER WITH PIERRE ROBIN SYNDROME
PIERRE ROBIN SYNDROME WITH HYPERPHALANGY AND CLINODACTYLY
INDEX FINGER ANOMALY WITH PIERRE ROBIN SYNDROME
PALATODIGITAL SYNDROME, CATEL-MANZKE TYPE
MICROGNATHIA DIGITAL SYNDROME
- (∗) Location:
- Chr.X
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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