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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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MAD deficiency, severe neonatal type
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18332 |
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hyperammonemia due to carbonic anhydrase VA deficiency
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14332 |
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16p11.2-p12.2 microdeletion syndrome
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13320 |
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16p11.2p12.2 microdeletion syndrome
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13320 |
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SDCCAG8 Senior-Loken syndrome
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13326 |
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piriformis muscle syndromes
|
43320 |
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congenital hematological system disease
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9332 |
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peripheral nervous system ganglioneuroblastoma
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3327 |
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peripheral nervous system ganglioneuroblastoma (disease)
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3327 |
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deep gluteal syndrome
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43320 |
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pelvic outlet syndrome
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43320 |
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piriformis muscle syndrome
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43320 |
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aase smith syndrome
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C535332 |
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Cranioectodermal dysplasia type 2
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13323 |
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cortical myoclonic tremor with epilepsy, familial, 3
|
13322 |
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