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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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BFNS2
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7366 |
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SDHx-related paraganglioma-pheochromocytoma
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17366 |
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familial pheochromocytoma-paraganglioma
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17366 |
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hereditary paraganglioma-pheochromocytoma
|
17366 |
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hereditary pheochromocytoma-paraganglioma
|
17366 |
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neu deficiency
|
C537366 |
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neu1 deficiency
|
C537366 |
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neug deficiency
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C537366 |
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sialidoses, type 2
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C537366 |
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benign neonatal seizures caused by mutation in KCNQ3
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7366 |
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type 2 sialidoses
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C537366 |
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type II sialidosis
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C537366 |
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type i sialidosis
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C537366 |
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convulsions, benign familial neonatal, 2
|
7366 |
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seizures, benign familial neonatal, 2
|
7366 |
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