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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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hereditary spastic paraplegia 48
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13342 |
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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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stuttering, familial persistent 1
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D013342 |
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RPE65 retinitis pigmentosa
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13425 |
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PDE6B retinitis pigmentosa
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13429 |
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endocrine active pituitary adenoma
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3429 |
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type II pneumocyte adenoma
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3427 |
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cardiac rupture, post infarction
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D006342 |
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heart rupture, post infarction
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D006342 |
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cardiac rupture, post-infarction
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D006342 |
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cardiac ruptures, post-infarction
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D006342 |
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heart rupture, post-infarction
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D006342 |
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heart ruptures, post-infarction
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D006342 |
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lyme disease, post-treatment
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D000077342 |
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