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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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laron type dwarfism 2
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C537871 |
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primary ciliary dyskinesia 29
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14378 |
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primary ciliary dyskinesia 29 without situs inversus
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14378 |
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primary ciliary dyskinesia caused by mutation in CCNO
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14378 |
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primary ciliary dyskinesia type 29
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14378 |
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dentin anomalous dysplasia
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D003784 |
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Tetra-amelia, ectodermal dysplasia, and lacrimal duct abnormality
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C537838 |
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coronal dentin dysplasias
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D003784 |
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dentin anomalous dysplasias
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D003784 |
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C8orf37 cone-rod dystrophy
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13786 |
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corneal endothelial dystrophy 1, autosomal dominant
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7378 |
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corneal endothelial dystrophy 1, autosomal dominant, formerly
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7378 |
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lattice corneal dystrophy type i
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C537881 |
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CDL1 corneal dystrophy, lattice type 1
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C537881 |
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macular corneal dystrophy, type i
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C537834 |
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