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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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familial isolated dilated cardiomyopathy caused by mutation in NEXN
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13147 |
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acquired communication disorders
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D003147 |
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childhood communication disorders
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D003147 |
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developmental communication disorders
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D003147 |
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neurogenic communication disorders
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D003147 |
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NEXN familial isolated dilated cardiomyopathy
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13147 |
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x-linked 31 mental retardation
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C563147 |
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communication disorders, neurogenic
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D003147 |
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Space adaptation syndrome
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3147 |
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space motion sickness
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3147 |
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fetal parainfluenza virus type 3 syndrome
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23147 |
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dilated cardiomyopathy type 1CC
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13147 |
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cardiomyopathy, dilated, type 1Cc
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13147 |
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mental retardation, x-linked 31
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C563147 |
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