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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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premature aging syndrome, Okamoto type
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11149.0 |
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ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
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9149.0 |
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microcephaly (disease)
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1149.0 |
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pure hereditary spastic paraplegia
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15149.0 |
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qualitative or quantitative defects of merosin
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16149.0 |
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pulmonary hypertension
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5149.0 |
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obsolete retinopathy
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149.0 |
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genetic vs non-genetic etiology
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21149.0 |
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fetal akinesia-cerebral and retinal hemorrhage syndrome
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14149.0 |
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encephalopathy, bovine spongiform
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25149.0 |
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cholesteryl ester storage disease
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19149.0 |
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rare eye disease due to a differentiation anomaly
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20149.0 |
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GM1 gangliosidosis
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18149.0 |
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obsolete aggressive systemic mastocytosis
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3149.0 |
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gallbladder pleomorphic giant cell adenocarcinoma
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4149.0 |
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