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
ADHCAI http://purl.obolibrary.org/obo/MONDO_0007538
AI3 http://purl.obolibrary.org/obo/MONDO_0007538
AI3A http://purl.obolibrary.org/obo/MONDO_0007538
autosomal dominant amelogenesis imperfecta hypocalcification type http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta caused by mutation in FAM83H http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta, hypocalcification type, autosomal dominant http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta hypomineralization type http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta, hypomineralization type http://purl.obolibrary.org/obo/MONDO_0007538
FAM83H amelogenesis imperfecta http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta type 3 http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta, type 3 http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta type 3A http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta, type 3A http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta type III http://purl.obolibrary.org/obo/MONDO_0007538
amelogenesis imperfecta, type III http://purl.obolibrary.org/obo/MONDO_0007538