|
ALDH18A1 autosomal dominant complex spastic paraplegia
|
15091 |
|
|
autosomal dominant complex spastic paraplegia caused by mutation in ALDH18A1
|
15091 |
|
|
cataracts, motor neuronopathy, short stature and skeletal abnormalities
|
15091 |
|
|
bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy
|
15091 |
|
|
autosomal dominant spastic paraplegia type 9
|
15091 |
|
|
spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome
|
15091 |
|
|
cataracts-motor neuropathy-short stature-skeletal anomalies syndrome
|
15091 |
|
|
autosomal dominant spastic paraparesis
|
15091 |
|
