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| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
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MONDO_prefferred_names from the Bioportal site.
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24,286 entries
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There is 0 pattern entry.
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orbital cyst
|
1915.0 |
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MHC class II deficiency
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8855.0 |
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HRPT3
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12406.0 |
|
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KTCN4
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12236.0 |
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rapadilino syndrome
|
9955.0 |
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ectodermal dysplasia, trichoodontoonychial type
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7511.0 |
|
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cleidorhizomelic syndrome
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7341.0 |
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syndactyly-telecanthus-anogenital and renal malformations syndrome
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10408.0 |
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myalgia-eosinophilia syndrome associated with tryptophan
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16822.0 |
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inherited organic acidemia
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688.0 |
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neuronal intestinal dysplasia
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858.0 |
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childhood-onset epilepsy syndrome
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20072.0 |
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ciliary discoordination due to random ciliary orientation
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8984.0 |
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deafness-onychodystrophy syndrome
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17922.0 |
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obsolete autosomal dominant cerebellar ataxia
|
1958.0 |
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