|
genetic cerebral small vessel disease
|
18787 |
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
C566878 |
|
|
anemia congenital sideroblastic B6-responsive
|
8786 |
|
|
pyridoxine refractory sideroblastic anemia
|
8785 |
|
|
anemia, congenital sideroblastic, B6-responsive
|
8786 |
|
|
pediatric multiple sclerosis
|
18784 |
|
|
amyotrophic lateral sclerosis 2
|
8780 |
|
|
amyotrophic lateral sclerosis 2, juvenile
|
8780 |
|
|
amyotrophic lateral sclerosis 2, juvenile; ALS2
|
http://purl.obolibrary.org/obo/MONDO_0008780 |
|
|
amyotrophic lateral sclerosis caused by mutation in ALS2
|
8780 |
|
|
amyotrophic lateral sclerosis type 2
|
8780.0 |
|
|
amyotrophic lateral sclerosis type 2, juvenile
|
8780 |
|
|
amyotrophic lateral sclerosis with polyglucosan bodies
|
8782 |
|
|
amyotrophic lateral sclerosis, juvenile, with dementia
|
8781 |
|
|
congenital laryngeal stridor
|
7878 |
|
