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
ALS 4976
COXPD31 14976
enzymopathy http://purl.obolibrary.org/obo/MONDO_0044976
Charcot disease 4976
progressive myoclonic 2b epilepsy C564976
enzyme disorder http://purl.obolibrary.org/obo/MONDO_0044976
disease of catalytic activity 44976.0
epilepsy, progressive myoclonic 2b C564976
iatrogenic Creutzfeldt-Jakob disease 34976
Lou Gehrig disease 4976
Lou Gehrig's disease 4976
motor neuron disease, bulbar 4976
MIPEP combined oxidative phosphorylation deficiency 14976
amyotrophic lateral sclerosis 4976
combined oxidative phosphorylation deficiency 31 14976