Phenotype #0000171857

Individual ID 00227851
Associated disease -
Phenotype details profound hearing loss; cochlear implant; mild motor delay; mild communicative delay; mild cognitive impairment; ventriculomegaly; corpus callosum posterior agenesis; heterotopia extensive; frontal polymicrogyria extensive; no cerebellar dysplasia; right cerebellopontine angle cysts
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name -