PubDictionaries

MONDO_bioport_pref_name

183,974 entries

Label	Id

hypertrophic cardiomyopathy 2	7266
negative surgical margin	D000072662
hypertrophic cardiomyopathy caused by mutation in TNNT2	7266
cardiomyopathy familial hypertrophic 2	7266
cardiomyopathy, familial hypertrophic, 2	7266
cardiomyopathy, familial hypertrophic, 2; CMH2	http://purl.obolibrary.org/obo/MONDO_0007266
cardiomyopathy, familial hypertrophic, type 2	7266
TNNT2 hypertrophic cardiomyopathy	7266
familial hypertrophic cardiomyopathy type 2	7266
deafness, autosomal dominant, due to mutation in Myo1a	C567266
autosomal dominant, due to mutation in Myo1a deafness	C567266
ectrodactyly, syndactyly, duplication of the great toes hydrops	C537266
margins of excision	D000072662
positive surgical margin	D000072662
negative surgical margins	D000072662