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
CMH12 12804
hypertrophic cardiomyopathy 12 12804
hypertrophic cardiomyopathy caused by mutation in CSRP3 12804
sinus node dysfunction D012804
CSRP3 hypertrophic cardiomyopathy 12804
sinus node disease D012804
sinus node dysfunctions D012804
sinus node diseases D012804
cardiomyopathy familial hypertrophic 12 12804
cardiomyopathy, familial hypertrophic, 12 12804
cardiomyopathy, familial hypertrophic, 12; CMH12 http://purl.obolibrary.org/obo/MONDO_0012804
cardiomyopathy, familial hypertrophic, type 12 12804
hypertrophic cardiomyopathy type 12 12804
dysfunction, sinus node D012804
dysfunctions, sinus node D012804