Phenotype #0000171855

Individual ID 00227849
Associated disease -
Phenotype details severe hearing loss; no hearing aid; no motor delay; communicative delay; mild cognitive impairment; shunted hydrocephalus; corpus callosum posterior agenesis; heterotopia small; frontal polymicrogyria extensive; cerebellar dysplasia; no arachnoid cysts, right ventricle herniation into midline
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name -