- OMIM ID
-
602066
- OMIM term:
- CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS; ICCA
- Alternative terms:
-
INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL
ICCA SYNDROME PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC
- (∗) Location:
- 16p12-q12
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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