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
CMH10 12112
hypertrophic cardiomyopathy 10 12112
cardiomyopathy, familial hypertrophic, 10 12112
MYL2 hypertrophic cardiomyopathy 12112
hypertrophic cardiomyopathy caused by mutation in MYL2 12112
cardiomyopathy, familial hypertrophic, 10; CMH10 http://purl.obolibrary.org/obo/MONDO_0012112
cardiomyopathy, familial hypertrophic, type 10 12112
cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 2 12112
hypertrophic cardiomyopathy type 10 12112