|
spinocerebellar ataxia 2; SCA2
|
http://purl.obolibrary.org/obo/MONDO_0008458 |
|
|
olivopontocerebellar atrophy, Holguin type
|
8458 |
|
|
familial benign hypercalcemia
|
18458 |
|
|
state, minimally conscious
|
D018458 |
|
|
states, minimally conscious
|
D018458 |
|
|
autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2
|
8458 |
|
|
ATXN2 autosomal dominant cerebellar ataxia type I
|
8458 |
|
|
familial hypocalciuric hypercalcemia
|
18458 |
|
|
familial benign hypocalciuric hypercalcemia
|
18458 |
|
|
unawareness state, post-comatose
|
D018458 |
|
|
unawareness state, postcomatose
|
D018458 |
|
