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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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stuttering, childhood
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D013342 |
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stuttering, developmental
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D013342 |
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familial persistent 1 stuttering
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D013342 |
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hereditary spastic paraplegia caused by mutation in AP5Z1
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13342 |
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hereditary spastic paraplegia type 48
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13342 |
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autosomal recessive spastic paraplegia type 48
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13342 |
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stuttering, familial persistent 1
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D013342 |
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AP5Z1 hereditary spastic paraplegia
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13342 |
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autosomal recessive spastic paraplegia 48
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13342 |
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benign Pericytic tumor
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3342 |
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benign perivascular tumor
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3342 |
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