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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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arthrogryposis multiplex congenita, distal, type i
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C535378 |
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nystagmus 1, congenital, x- linked
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C537853 |
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nystagmus 1, congenital, x-linked
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C537853 |
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westerhof beemer cormane syndrome
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C537836 |
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macular type corneal dystrophy
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C537834 |
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posterior polymorphous corneal dystrophy 1
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7378 |
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LCD1 lattice corneal dystrophy 1
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C537881 |
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posterior polymorphous corneal dystrophy type 1
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7378 |
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congenital nystagmus, corneal pannus, and presenile cataracts foveal hypoplasia
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C537858 |
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dentin dysplasias, coronal
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D003784 |
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mal de debarquement
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C537840 |
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mal de debarquement syndrome
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C537840 |
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hyperthermia induced defects
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16378 |
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T lymphocyte deficiency
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3780 |
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17-hydroxysteroid dehydrogenase deficiency
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C537805 |
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