All diseases

OMIM ID
606155
OMIM term:
FRYNS-AFTIMOS SYNDROME
Alternative terms:
PACHYGYRIA, MENTAL RETARDATION, EPILEPSY, AND CHARACTERISTIC FACIES
CEREBROOCULOFACIAL LYMPHATIC SYNDROME
COFL SYNDROME
MENTAL RETARDATION WITH EPILEPSY AND CHARACTERISTIC FACIES
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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