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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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tremor, hereditary essential, 5
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14756.0 |
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early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome
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44646.0 |
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anomaly of the tricuspid valve chordae
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20396.0 |
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benign neoplasm of lip
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21496.0 |
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Skint1-like pseudogene
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14616.0 |
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Bardet-Biedl syndrome 18
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14446.0 |
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malignant catarrh
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25096.0 |
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megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
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18436.0 |
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ataxia - telangiectasia variant
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18266.0 |
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prostate calculus
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1776.0 |
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Fanconi anemia complementation group L
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13566.0 |
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duodenal atresia (disease)
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9126.0 |
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membranous glomerulonephritis
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5376.0 |
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angioleiomyoma
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6646.0 |
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undifferentiated gallbladder carcinoma
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6476.0 |
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