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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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choroidal dystrophy, central areolar 3
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C567729 |
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dilated, 1DD cardiomyopathy
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C567725 |
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dilated, 1CC cardiomyopathy
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C567733 |
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atopic, 7 dermatitis
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C567796 |
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primary congenital, d glaucoma 3
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C567765 |
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combined mitochondrial complex deficiency
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C567769 |
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platelet cox1 deficiency
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C567786 |
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mitochondrial complex deficiency, combined
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C567769 |
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night blindness, congenital stationary, type 1c
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C567704 |
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neutropenia, severe congenital, autosomal dominant 2
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C567748 |
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muscular dystrophy, congenital, due to integrin alpha-7 deficiency
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C567709 |
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muscular dystrophy, congenital, lmna-related
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C567708 |
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46,xy, cbx2-related disorder of sex development
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C567766 |
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ren-related kidney disease
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C567760 |
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macrothrombocytopenia, autosomal dominant, tubb1-related
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C567747 |
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