Mondo_2019_Kim Find_IDs Find_Terms Annotation
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created at 2021-12-20 07:01:32 UTC
updated at 2021-12-22 01:40:39 UTC
Mondo_2019_Kim from bioportal
113,078 entries
Label
Id
AI1B http://purl.obolibrary.org/obo/MONDO_0007092
AIH2 http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta caused by mutation in ENAM http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta caused by mutation in enam http://purl.obolibrary.org/obo/MONDO_0007092
hereditary localized enamel hypoplasia http://purl.obolibrary.org/obo/MONDO_0007092
ENAM amelogenesis imperfecta http://purl.obolibrary.org/obo/MONDO_0007092
enamel hypoplasia, hereditary localized http://purl.obolibrary.org/obo/MONDO_0007092
autosomal dominant hypoplastic local amelogenesis imperfecta http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta, hypoplastic local, autosomal dominant http://purl.obolibrary.org/obo/MONDO_0007092
enam amelogenesis imperfecta http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta type IB http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta, type IB http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta, type IB; AI1B http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta type 1B http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta, type 1B http://purl.obolibrary.org/obo/MONDO_0007092