|
autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation
|
14711 |
|
|
autosomal dominant Charcot-Marie-Tooth disease type 2W
|
14711 |
|
|
autosomal dominant axonal Charcot-Marie-Tooth disease type 2W
|
14711 |
|
|
Charcot-Marie-Tooth disease, axonal type 2W
|
14711 |
|
|
Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2W
|
14711 |
|
|
Charcot-Marie-Tooth disease, axonal, type 2W
|
14711 |
|
|
Charcot-Marie-Tooth disease, axonal, type 2W; CMT2W
|
http://purl.obolibrary.org/obo/MONDO_0014711 |
|
|
Charcot-Marie-Tooth disease, axonal, type 2w
|
14711 |
|
|
artery insufficiencies, basilar
|
D014715 |
|
|
Senior-Loken syndrome 9; SLSN9
|
14712 |
|
|
SMITH-Kingsmore syndrome; SKS
|
http://purl.obolibrary.org/obo/MONDO_0014716 |
|
|
artery insufficiency, basilar
|
D014715 |
|
