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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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mental retardation Smith Fineman Myers type
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19778 |
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craniofrontonasal dysplasia, Teebi type
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7780 |
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q fevers, acute
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D011778 |
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cone-rod dystrophy and hearing loss 1
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20778 |
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syndromes, short bowel
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D012778 |
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cone-rod dystrophy, aipl1-related
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C565778 |
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deficiency syndrome, antibody
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3778 |
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deficiency syndromes, antibody
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3778 |
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leber congenital amaurosis 4
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C565778 |
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hereditary transthyretin amyloidosis
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C567782 |
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hereditary, transthyretin-related amyloidosis
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C567782 |
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amyloidosis, cutaneous bullous
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8778 |
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fever, coxiella burnetii
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D011778 |
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fevers, coxiella burnetii
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D011778 |
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infection, coxiella burnetii
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D011778 |
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