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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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chronic granulomatous disease caused by mutation in NCF2
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9310 |
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inverse recessive dystrophic epidermolysis bullosa
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19310 |
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distal muscular dystrophies
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D049310 |
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tibial muscular dystrophies
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D049310 |
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finnish-markesbery muscular dystrophy
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D049310 |
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udd-markesbery muscular dystrophy
|
D049310 |
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muscular dystrophy, finnish-markesbery
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D049310 |
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distal 1 myopathies
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D049310 |
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late distal hereditary myopathy
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D049310 |
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distal myopathy markesbery griggs type
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D049310 |
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distal myopathy markesbery-griggs type
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D049310 |
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distal myopathy, laing
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D049310 |
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finnish markesbery muscular dystrophy
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D049310 |
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udd markesbery muscular dystrophy
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D049310 |
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distal 1 myopathy
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D049310 |
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