478
Mutations in the human EGR2 gene have recently been associated with the inherited peripheral neuropathies Charcot - Marie - Tooth type 1 , Dejerine - Sottas syndrome and congenital hypomyelinating neuropathy .
 Disease: inherited peripheral neuropathies; Disease: Charcot - Marie - Tooth type 1; Disease: Dejerine - Sottas syndrome; Disease: congenital hypomyelinating neuropathy
Given options, please tell me the categories of all the listed entity words.Output format is "type1: word1; type2: word2". 
Option: Disease 
Text: {0} 
 Entities: inherited peripheral neuropathies, Charcot - Marie - Tooth type 1, Dejerine - Sottas syndrome, congenital hypomyelinating neuropathy 
Answer:
 Disease: inherited peripheral neuropathies; Disease: Charcot - Marie - Tooth type 1; Disease: Dejerine - Sottas syndrome; Disease: congenital hypomyelinating neuropathy