Congenital cataracts - facial dysmorphism - neuropathy

• CCFDN

• Rare palpebral disease
• Spinocerebellar ataxia with oculomotor anomaly
• Early-onset ataxia with dementia
• Rare hereditary ataxia
• Cerebral disease with cataract
• Cerebellar ataxia with peripheral neuropathy
• Syndromic developmental defect of the eye
• hereditary motor neuron disease
• Rare genetic intellectual disability with developmental anomaly
• has_disease_location some motor neuron