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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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familial hemiplegic migraine
|
700.0 |
|
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autoimmune glomerulonephritis
|
30700.0 |
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hawkinsinuria
|
7700.0 |
|
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neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to a point mutation
|
14700.0 |
|
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SIN3A-related intellectual disability syndrome due to a point mutation
|
44700.0 |
|
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obsolete pseudohypoparathyroidism without Albright hereditary osteodystrophy
|
18700.0 |
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obsolete microcephaly, short stature, and impaired glucose metabolism
|
20700.0 |
|
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pancreatic triacylglycerol lipase deficiency
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13700.0 |
|
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brachial plexus neoplasm
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3700.0 |
|
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orbital dermoid cyst
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40700.0 |
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obsolete epithelioid trophoblastic tumor
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2700.0 |
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anaplastic ependymoma
|
16700.0 |
|
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glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
|
17700.0 |
|
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choroid cancer
|
6700.0 |
|
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proteasome-associated autoinflammatory syndrome 2
|
54700.0 |
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