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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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mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6
|
32869.0 |
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partial deletion of chromosome 4
|
16869.0 |
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heart valve disease
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2869.0 |
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epidermolysis bullosa simplex superficialis
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11869.0 |
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isolated Pierre-Robin syndrome
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9869.0 |
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coronary arteries congenital malformation
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22869.0 |
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nondystrophic myotonia
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54869.0 |
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obsolete rare benign breast tumor
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15869.0 |
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paraurethral gland cancer
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1869.0 |
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