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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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Protein S deficiency
|
2304 |
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Protein S deficiency disease
|
2304 |
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protein S deficiency
|
2304 |
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central auditory disease
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D001304 |
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lactate dehydrogenase deficiency type A
|
13047 |
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glycogen storage disease 13
|
13046 |
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glycogen storage disease caused by mutation in LDHA
|
13047 |
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arachnoid mater inflammation
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15304 |
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von Willebrand disease 2
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13304 |
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glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
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13047 |
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von willebrand's disease 2
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13304 |
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glycogen storage disease XI
|
13047 |
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glycogen storage disease due to muscle beta-enolase deficiency
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13046 |
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glycogen storage disease XI; GSD11
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http://purl.obolibrary.org/obo/MONDO_0013047 |
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glycogen storage disease XIII
|
13046 |
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