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| license |
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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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nervous system diseases, parasympathetic
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D001342 |
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classic complement early component deficiency caused by mutation in C8B
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13421 |
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autonomic peripheral nervous system diseases
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D001342 |
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peripheral autonomic nervous system diseases
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D001342 |
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aneurysm - osteoarthritis syndrome
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13426 |
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CMP-sialic acid transporter deficiency
|
11342 |
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C8 deficiency, type 2
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13421 |
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Meier-Gorlin syndrome type 2
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13428 |
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retinitis pigmentosa type 20
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13425 |
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Loeys-Dietz syndrome type 3
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13426 |
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Loeys-Dietz syndrome, type 3
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13426 |
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distal monosomy type 3p
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13424 |
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retinitis pigmentosa type 40
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13429 |
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autonomic nervous system diseases
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D001342 |
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parasympathetic nervous system diseases
|
D001342 |
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