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| license |
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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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CHED
|
9019 |
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CHED2
|
9019 |
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CHEDII
|
9019 |
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OI
|
19019 |
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Osteopsathyrosis
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19019 |
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Fragilitas ossium
|
19019 |
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Lobstein disease
|
19019 |
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Lobstein's syndrome
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19019 |
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Vrolik disease
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19019 |
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Vrolik's disease
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19019 |
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osteogenesis imperfecta
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19019 |
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CHED2, formerly
|
9019 |
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Porak and Durante disease
|
19019 |
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corneal dystrophy, congenital hereditary endothelial
|
9019 |
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autosomal recessive CHED
|
9019 |
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