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
trisomy 5p13 13169
nephronophthisis (disease) caused by mutation in XPNPEP3 13163
Parkinson disease 16 13167
parkinson disease 16 13167
Parkinson disease 16; PARK16 http://purl.obolibrary.org/obo/MONDO_0013167
nephronophthisis-like nephropathy 1; NPHPL1 http://purl.obolibrary.org/obo/MONDO_0013163
cardiomyopathy, dilated, 1DD 13168
dilated cardiomyopathy 1DD 13168
cardiomyopathy, dilated, 1DD; CMD1DD http://purl.obolibrary.org/obo/MONDO_0013168
gamma aminobutyric acid transaminase deficiency 13166
gamma-amino butyric acid transaminase deficiency 13166
cancer, spleen D013160
cancer, splenic D013160
cancers, spleen D013160
cancers, splenic D013160