| manager |
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| language |
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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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sensorineural hearing loss
|
20678 |
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sensorineural hearing loss disorder
|
20678 |
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Fukuyama congenital muscular dystrophy
|
9678 |
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myofibrillar, bag3-related myopathy
|
C567843 |
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autosomal dominant mental retardation 39
|
14678 |
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inborn pyruvate metabolic process disorder
|
16789 |
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paternal 14q32.2 microdeletion syndrome
|
16780 |
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maternal 14q32.2 microdeletion syndrome
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16781 |
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centralis diffusa, myelinosis
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D056784 |
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complete hydatidiform mole
|
16785 |
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incomplete hydatidiform mole
|
16786 |
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partial hydatidiform mole
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16786 |
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benign axillary neoplasm
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36781 |
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toxoplasmosis, central nervous system
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D016781 |
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infections, gram negative bacterial
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21678 |
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