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
CMH13 13195
hypertrophic cardiomyopathy 13 13195
hypertrophic cardiomyopathy caused by mutation in TNNC1 13195
cardiomyopathy familial hypertrophic 13 13195
cardiomyopathy, familial hypertrophic, 13 13195
cardiomyopathy, familial hypertrophic, 13; CMH13 http://purl.obolibrary.org/obo/MONDO_0013195
cardiomyopathy, familial hypertrophic, type 13 13195
hypertrophic cardiomyopathy type 13 13195
TNNC1 hypertrophic cardiomyopathy 13195