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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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brachydactyly type a6
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C537092 |
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brachydactyly, type a6
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C537092 |
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macular degeneration, dry
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D057092 |
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type a6 brachydactyly
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C537092 |
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erythropoietic porphyria, congenital
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D017092 |
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erythropoietic porphyrias, congenital
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D017092 |
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porphyria, erythropoietic, congenital
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D017092 |
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dry macular degeneration
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D057092 |
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dry macular degenerations
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D057092 |
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amelogenesis imperfecta caused by mutation in ENAM
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7092 |
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amelogenesis imperfecta caused by mutation in enam
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7092 |
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macular degenerations, dry
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D057092 |
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porphyrias, congenital erythropoietic
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D017092 |
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hereditary localized enamel hypoplasia
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7092 |
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autosomal dominant hypoplastic local amelogenesis imperfecta
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7092 |
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