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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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KCNV2-Related cone dystrophy with night blindness and supernormal rod responses
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C563678 |
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nocturnal frontal lobe, type 4 epilepsy
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C563679 |
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familial, with nocturnal wandering and ictal fear epilepsy
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C563679 |
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diffuse corticomeningeal, of divry and van bogaert angiomatosis
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C536367 |
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polymyositis with skin involvement
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16367 |
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pharyngeal adenoid cystic carcinoma
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6367 |
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pharynx adenoid cystic carcinoma
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6367 |
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malabsorptive, congenital diarrhea 4
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C563673 |
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age-related, 6 macular degeneration
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C563674 |
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epilepsy, familial, with nocturnal wandering and ictal fear
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C563679 |
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