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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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hereditary keratitis
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7848 |
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keratitis, hereditary
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7848 |
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keratitis, autosomal dominant
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7848 |
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partial deletion of chromosome 12p
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17848 |
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lissencephaly syndrome, norman-roberts type
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C537848 |
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norman roberts lissencephaly syndrome
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C537848 |
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norman-roberts type lissencephaly syndrome
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C537848 |
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autosomal dominant keratitis
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7848 |
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dominantly inherited keratitis
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7848 |
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partial monosomy of chromosome 12p
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17848 |
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partial deletion of the short arm of chromosome 12
|
17848 |
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partial monosomy of the short arm of chromosome 12
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17848 |
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partial deletion of the short arm of chromosome type 12
|
17848 |
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