All diseases

OMIM ID
269720
OMIM term:
SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE
Alternative terms:
BFNS, AUTOSOMAL RECESSIVE
CONVULSIONS, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE
EPILEPSY, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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