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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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RNF213 Moyamoya disease
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11784 |
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intervertebral joint disease
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37847 |
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vertebral joint disease
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37847 |
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white matter disease
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D056784 |
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intervertebral joint disease or disorder
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37847 |
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white matter diseases
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D056784 |
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disease or disorder of intervertebral joint
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37847 |
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ophthalmoplegic neuromuscular disorder with abnormal mitochondria
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9784 |
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blood vessel dissection
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D000784 |
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aortic aneurysm-aortic dissection and patent ductus arteriosus
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C537784 |
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keratitis, autosomal dominant
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7848 |
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fatal infantile, due to cytochrome c oxidase deficiency cardioencephalomyopathy
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C565784 |
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hyperthyroidism, familial, due to inappropriate thyrotropin secretion
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7784 |
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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
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15784 |
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dentin anomalous dysplasia
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D003784 |
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