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Summary Literature (0)
MIM:610042 - PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1

Xenbase Genes: cntnap2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012400 - cortical dysplasia-focal epilepsy syndrome
MONDO:0016377 - Pitt-Hopkins-like syndrome

Disease Ontology (DO):
DOID:0090130 - cortical dysplasia-focal epilepsy syndrome