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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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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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cortex disorders, auditory
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D001304 |
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dysfunction, central auditory
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D001304 |
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dysfunctions, central auditory
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D001304 |
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familial cerebral cavernous malformation caused by mutation in CCM2
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11304 |
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CCM2 familial cerebral cavernous malformation
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11304 |
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spastic quadriplegic cerebral palsy 3
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13048 |
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auditory diseases, central
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D001304 |
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auditory dysfunction, central
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D001304 |
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lactate dehydrogenase deficiency type A
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13047 |
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enolase 3 deficiency
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13046 |
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muscle enolase deficiency
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13046 |
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muscular enolase deficiency
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13046 |
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LDH-M subunit deficiency
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13047 |
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