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
Fanconi renotubular syndrome 1; FRTS1 http://purl.obolibrary.org/obo/MONDO_0024525
combined oxidative phosphorylation defect type 23 14525
combined oxidative phosphorylation deficiency 23 14525
combined oxidative phosphorylation deficiency 23; COXPD23 http://purl.obolibrary.org/obo/MONDO_0014525
combined oxidative phosphorylation deficiency caused by mutation in GTPBP3 14525
combined oxidative phosphorylation deficiency type 23 14525
Fanconi renotubular syndrome 24525
renal Fanconi syndrome 24525
dyserythropoietic anemia with thrombocytopenia C564525
Fanconi syndrome without cystinosis 24525