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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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spastic paraplegia 50, autosomal recessive; SPG50
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http://purl.obolibrary.org/obo/MONDO_0013048 |
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D-HUS with I factor anomaly
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13041 |
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D-HUS with B factor anomaly
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13042 |
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aHUS with B factor anomaly
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13042 |
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D-HUS with C3 anomaly
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13043 |
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aHUS with C3 anomaly
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13043 |
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lactate dehydrogenase A deficiency
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13047 |
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aHUS with I factor anomaly
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13041 |
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CCM2 familial cerebral cavernous malformation
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11304 |
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susceptibility to atypical hemolytic uremic syndrome 2
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13040 |
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susceptibility to atypical hemolytic uremic syndrome 3
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13041 |
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susceptibility to atypical hemolytic uremic syndrome 4
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13042 |
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susceptibility to atypical hemolytic uremic syndrome 5
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13043 |
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susceptibility to atypical hemolytic uremic syndrome 6
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13044 |
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cortex disorder, auditory
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D001304 |
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