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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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type i opitz-g syndrome
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C567932 |
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opitz BBBG syndrome, type i
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C567932 |
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opitz GBBB syndrome, type i
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C567932 |
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opitz GBBB syndrome, x-linked
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C567932 |
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myofibrillar myopathy, filamin C-related
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C537932 |
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myopathy, myofibrillar, filamin c-related
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C537932 |
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autosomal dominant filaminopathy
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C537932 |
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age related macular degeneration 2
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7932 |
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age related macular degeneration type 2
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7932 |
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filamin C-related myofibrillar myopathy
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C537932 |
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muscular hypertrophy-hepatomegaly-polyhydramnios syndrome
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17932 |
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opitz-g syndrome, type i
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C567932 |
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opitz syndrome, x-linked
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C567932 |
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