|
spastic paraplegia 9A, autosomal dominant
|
11006 |
|
|
spastic paraplegia 9A, autosomal dominant; SPG9A
|
http://purl.obolibrary.org/obo/MONDO_0011006 |
|
|
autosomal dominant complex spastic paraplegia type 9A
|
11006 |
|
|
intestinalis, pneumatosis cystoides
|
D011006 |
|
|
cataracts with motor neuronopathy, short stature and skeletal abnormalities
|
11006 |
|
|
cataracts with motor neuronopathy, short stature, and skeletal abnormalities
|
11006 |
|
|
cataracts motor neuropathy-short stature-skeletal anomalies syndrome
|
11006 |
|
|
hereditary spastic paraplegia 9A
|
11006 |
|
|
hereditary spastic paraplegia type 9A
|
11006 |
|
|
cystoides intestinalis, pneumatosis
|
D011006 |
|
|
autosomal dominant spastic paraplegia 9A
|
11006 |
|
|
spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux
|
11006 |
|
|
spastic paraparesis with amyopathy, cataracts, and gastroesophageal reflux
|
11006 |
|
