Mondo_2019_Kim Find_IDs Find_Terms Annotation
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created at 2021-12-20 07:01:32 UTC
updated at 2021-12-22 01:40:39 UTC
Mondo_2019_Kim from bioportal
113,078 entries
Label
Id
ALS13 http://purl.obolibrary.org/obo/MONDO_0008458
OPCA2 http://purl.obolibrary.org/obo/MONDO_0008458
SCA2 http://purl.obolibrary.org/obo/MONDO_0008458
SCA 2 http://purl.obolibrary.org/obo/MONDO_0008458
Wadia-swami syndrome http://purl.obolibrary.org/obo/MONDO_0008458
olivopontocerebellar atrophy 2 http://purl.obolibrary.org/obo/MONDO_0008458
spinocerebellar ataxia 2 http://purl.obolibrary.org/obo/MONDO_0008458
spinocerebellar atrophy 2 http://purl.obolibrary.org/obo/MONDO_0008458
spinocerebellar ataxia 2; SCA2 http://purl.obolibrary.org/obo/MONDO_0008458
spinocerebellar ataxia Cuban type http://purl.obolibrary.org/obo/MONDO_0008458
spinocerebellar ataxia, Cuban type http://purl.obolibrary.org/obo/MONDO_0008458
olivopontocerebellar atrophy Holguin type http://purl.obolibrary.org/obo/MONDO_0008458
olivopontocerebellar atrophy, Holguin type http://purl.obolibrary.org/obo/MONDO_0008458
autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2 http://purl.obolibrary.org/obo/MONDO_0008458
ATXN2 autosomal dominant cerebellar ataxia type I http://purl.obolibrary.org/obo/MONDO_0008458