hereditary spastic paraplegia 6
|
10878 |
|
spastic paraplegia 6, autosomal dominant
|
10878 |
|
spastic paraplegia 6, autosomal dominant; SPG6
|
http://purl.obolibrary.org/obo/MONDO_0010878 |
|
autosomal dominant familial spastic paraplegia type 3
|
10878 |
|
familial spastic paraplegia autosomal dominant 3
|
10878 |
|
hereditary spastic paraplegia caused by mutation in NIPA1
|
10878 |
|
hereditary spastic paraplegia type 6
|
10878 |
|
familial spastic paraplegia, autosomal dominant, 3
|
10878 |
|
autosomal dominant spastic paraplegia type 6
|
10878 |
|
NIPA1 hereditary spastic paraplegia
|
10878 |
|
autosomal dominant spastic paraplegia 6
|
10878 |
|