|
bile acid synthesis defect, congenital, type 1
|
11906 |
|
|
Charcot-Marie-Tooth disease type 1 caused by mutation in NEFL
|
11902 |
|
|
Charcot-Marie-Tooth disease type 1F
|
11902 |
|
|
Charcot-Marie-Tooth neuropathy type 1F
|
11902 |
|
|
Charcot-Marie-Tooth neuropathy, type 1F
|
11902 |
|
|
Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities
|
11903 |
|
|
Charcot-Marie-Tooth disease, type 2, with hearing loss and pupillary abnormalities
|
11903 |
|
|
Charcot-Marie-Tooth disease type 2H
|
11901 |
|
|
Charcot-Marie-Tooth disease type 2J
|
11903 |
|
|
Charcot-Marie-Tooth neuropathy type 2J
|
11903 |
|
|
Charcot-Marie-Tooth neuropathy, type 2J
|
11903 |
|
