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

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Label
Id
AI1G http://purl.obolibrary.org/obo/MONDO_0008771
AIGFS http://purl.obolibrary.org/obo/MONDO_0008771
ers http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta and gingival fibromatosis syndrome http://purl.obolibrary.org/obo/MONDO_0008771
enamel-renal syndrome http://purl.obolibrary.org/obo/MONDO_0008771
enamel-renal-gingival syndrome http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta and nephrocalcinosis http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta caused by mutation in FAM20A http://purl.obolibrary.org/obo/MONDO_0008771
generalized enamel hypoplasia and renal dysfunction http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta hypoplastic type, Ig http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta hypoplastic with nephrocalcinosis http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta, hypoplastic, with nephrocalcinosis http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta nephrocalcinosis http://purl.obolibrary.org/obo/MONDO_0008771
absent enamel, nephrocalcinosis and apparently normal calcium metabolism http://purl.obolibrary.org/obo/MONDO_0008771
amelogenesis imperfecta-nephrocalcinosis syndrome http://purl.obolibrary.org/obo/MONDO_0008771
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