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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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Gilchrist's disease
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5672 |
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blastomycotic infection
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5672 |
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CD79B deficiency
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C567200 |
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drayer syndrome
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C567232 |
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adiponectin deficiency
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C567258 |
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myopia 16
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C567259 |
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dursun syndrome
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C567260 |
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1q21.1 deletion
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C567291 |
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WAGRO syndrome
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C567292 |
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intracranial berry, 10 aneurysm
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C567237 |
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familial febrile, 10 seizures
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C567218 |
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autosomal recessive 1b deafness
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C567213 |
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1.35-mb chromosome 1q21.1 deletion syndrome
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C567291 |
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autosomal dominant 2b deafness
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C567214 |
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autosomal dominant 3 mental retardation
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C567241 |
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