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Summary Literature (0)
MIM:607341 - FOCAL CORTICAL DYSPLASIA, TYPE II; FCORD2

Xenbase Genes: tsc1, mtor, tsc2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011818 - superficial fascia
MONDO:0017101 - isolated focal cortical dysplasia type IIa
MONDO:0017102 - isolated focal cortical dysplasia type IIb
MONDO:0019009 - isolated focal cortical dysplasia