- OMIM ID
-
607341
- OMIM term:
- FOCAL CORTICAL DYSPLASIA OF TAYLOR; FCDT
- Alternative terms:
-
CORTICAL DYSPLASIA OF TAYLOR; CDT
FOCAL CORTICAL DYSPLASIA, TYPE II FOCAL CORTICAL DYSPLASIA OF TAYLOR, TYPE IIA, INCLUDED
CORTICAL DYSPLASIA OF TAYLOR WITHOUT BALLOON CELLS, INCLUDED
CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY, INCLUDED; CDTD, INCLUDED
FOCAL CORTICAL DYSPLASIA OF TAYLOR, TYPE IIB, INCLUDED
CORTICAL DYSPLASIA OF TAYLOR WITH BALLOON CELLS, INCLUDED; CDTBC, INCLUDED
- (∗) Location:
- 9q34.13
- (†) Associated OMIM genes:
- TSC1
- (‡) Associated MGI genes:
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