MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
ADSA 12166
Adsa 12166
SNAX1 12166
ataxia, sensory, 1, autosomal dominant 12166
ataxia, sensory, 1, autosomal dominant; SNAX1 http://purl.obolibrary.org/obo/MONDO_0012166
hereditary ataxia caused by mutation in RNF170 12166
hemorrhage, retinal D012166
retinal hemorrhage D012166
retinal hemorrhages D012166
RNF170 hereditary ataxia 12166
autosomal dominant sensory ataxia 1 12166