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| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
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MONDO_prefferred_names from the Bioportal site.
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24,286 entries
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There is 0 pattern entry.
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severe early-onset axonal neuropathy due to MFN2 deficiency
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19549.0 |
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cork-handlers' disease
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4549.0 |
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adenosquamous bile duct carcinoma
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3549.0 |
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late-onset scapuloperoneal muscular dystrophy with hyaline bodies
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18549.0 |
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Charcot-Marie-Tooth disease X-linked dominant 1
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10549.0 |
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thoracic dysostosis, isolated
|
8549.0 |
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hypotrichosis 1
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11549.0 |
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severe early-childhood-onset retinal dystrophy
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9549.0 |
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MCOPCB1
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24549.0 |
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generalized dominant dystrophic epidermolysis bullosa
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7549.0 |
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lethal congenital contracture syndrome 6
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14549.0 |
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invasive hydatidiform mole
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20549.0 |
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N-acetylaspartate deficiency
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13549.0 |
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optic atrophy 12
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33549.0 |
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peroxisome biogenesis disorder 10b
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54549.0 |
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