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| language |
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| license |
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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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autosomal dominant cerebellar ataxia type 3
|
19793 |
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autosomal dominant cerebellar ataxia type 4
|
19794 |
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autosomal dominant cerebellar ataxia type I
|
19792 |
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autosomal dominant cerebellar ataxia type III
|
19793 |
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autosomal dominant cerebellar ataxia type IV
|
19794 |
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benign hereditary chorea
|
8979 |
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RSPH9 primary ciliary dyskinesia
|
12979 |
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LRRC6 primary ciliary dyskinesia
|
13979 |
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thoracic outlet compression syndrome
|
5979 |
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ornithine aminotransferase deficiency
|
9796 |
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UMP synthtase deficiency
|
9797 |
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Ump synthase deficiency
|
9797 |
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orotidylic decarboxylase deficiency
|
9797 |
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unusual facies, digital abnormalities, and ichthyosis
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9792 |
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ichthyosis-oral and digital anomalies syndrome
|
9792 |
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