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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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ciliary dyskinesia, primary, type 19
|
13979 |
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autoimmune lymphoproliferative syndrome type 1, autosomal dominant
|
17979 |
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Clayton Smith-Donnai syndrome
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9792 |
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long QT syndrome type 8
|
10979 |
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long QT syndrome with syndactyly
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10979 |
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Pure cerebellar syndrome-mild pyramidal signs syndrome
|
19793 |
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uridine monophosphate synthase deficiency
|
9797 |
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uridine monophosphate synthetase deficiency
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9797 |
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long QT syndrome-syndactyly syndrome
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10979 |
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congenital, refractory to acetylcholinesterase inhibitors myasthenia
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C564979 |
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cystadenoma of the intrahepatic bile duct
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3979 |
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TOS - thoracic outlet syndrome
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5979 |
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hereditary predisposition to infections
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15979.0 |
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oral-Facial-digital syndrome, type 3
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9793 |
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orotic aciduria type 1
|
9797 |
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