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
MMIT 10780
benign COX deficiency 10780
Cox deficiency myopathy, infantile, transient 10780
reversible infantile cytochrome C oxidase deficiency 10780
infantile reversible cytochrome C oxidase deficiency myopathy 10780
mitochondrial myopathy, infantile, transient 10780
mitochondrial myopathy, infantile, transient, due to respiratory chain deficiency 10780
mitochondrial myopathy, infantile, transient; MMIT http://purl.obolibrary.org/obo/MONDO_0010780
respiratory chain deficiency, infantile, transient 10780
reversible infantile respiratory chain deficiency 10780
mitochondrial myopathy with reversible COX deficiency 10780
mitochondrial myopathy with reversible complex IV deficiency 10780
mitochondrial myopathy with reversible cytochrome C oxidase deficiency 10780