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