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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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dystonic disorder caused by mutation in HPCA
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9141 |
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Meier-Gorlin syndrome caused by mutation in ORC1
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9143 |
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Pure or complicated autosomal dominant spastic paraplegia
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17914 |
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celiac artery compression syndrome
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4914 |
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fiber-type disproportion, congenital
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D020914 |
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deficiency of cholesterol esterase and triacylglycerol lipase
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19148 |
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blomstrand type chondrodysplasia
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C537914 |
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fiber-type disproportions, congenital
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D020914 |
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myopathies, structural, congenital
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D020914 |
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non-progressive myopathies, congenital
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D020914 |
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non-progressive myopathy, congenital
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D020914 |
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structural myopathies, congenital
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D020914 |
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structural myopathy, congenital
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D020914 |
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Protein C deficiency disease
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19145 |
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protein C deficiency
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19145 |
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