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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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lissencephaly syndrome, norman-roberts type
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C537848 |
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congenital progressive oculo-acoustico-cerebral degeneration
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C537849 |
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calcifications, dental pulp
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D003784 |
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stone, dental pulp
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D003784 |
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stones, dental pulp
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D003784 |
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dentin dyspalsia, shields type 2
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D003784 |
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congenital, autosomal recessive methemoglobinemia
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C537841 |
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nadh-cytochrome b5 reductase deficiency
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C537841 |
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nadh-cytochrome b5 reductase deficiency, type i
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C537841 |
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nadh-cytochrome b5 reductase deficiency, type ii
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C537841 |
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lethal neonatal rigidity-multifocal seizure syndrome
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13784 |
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dentin dysplasia, shields type II
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D003784 |
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dental pulp stone
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D003784 |
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carcinoma in situ of nasal cavities
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3784 |
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carcinoma in situ of nasal cavity
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3784 |
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