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
LDH-M subunit deficiency 13047
glycogen storage disease due to lactate dehydrogenase M-subunit deficiency 13047
central auditory disease D001304
glycogen storage disease due to muscle beta-enolase deficiency 13046
glycogen storage disease type 11 13047
glycogen storage disease type 13 13046
hypertensive renal disease, benign 1304
glycogen storage disease 13 13046
glycogen storage disease XI 13047
glycogen storage disease XI; GSD11 http://purl.obolibrary.org/obo/MONDO_0013047
glycogen storage disease XIII 13046
glycogen storage disease XIII; GSD13 http://purl.obolibrary.org/obo/MONDO_0013046
hypertensive renal disease, benign, without mention of renal failure 1304
central auditory diseases D001304
auditory cortex disorder D001304