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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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pterygium syndrome, multiple, autosomal dominant
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8338 |
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ATP7A spinal muscular atrophy
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10338 |
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severe combined immunodeficiency with hypereosinophilia
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11338 |
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congenital, with microcornea or slight microphthalmia cataract
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C535338 |
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fatal multiple mitochondrial dysfunction syndrome
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17338 |
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fatal multiple mitochondrial dysfunctions syndrome
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17338 |
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Hirschsprung disease modifier
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13383 |
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ATP7A-related distal motor neuropathy
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10338 |
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multiple cranial neuropathies
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D003389 |
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palsies, cranial nerve
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D003389 |
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palsy, cranial nerve
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D003389 |
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inflammation, vestibular nerve
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D020338 |
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inflammations, vestibular nerve
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D020338 |
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neuritides, vestibular nerve
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D020338 |
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neuritis, vestibular nerve
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D020338 |
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