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| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
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MONDO_prefferred_names from the Bioportal site.
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24,286 entries
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There is 0 pattern entry.
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corneal dystrophy pigmentary anomaly malabsorption
|
22866.0 |
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myoglobinuria
|
866.0 |
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bipolar I disorder
|
1866.0 |
|
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mosaic trisomy 5
|
19866.0 |
|
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nasopharyngeal diphtheria
|
20866.0 |
|
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mycobacterium avium complex disease
|
5866.0 |
|
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Charcot-Marie-Tooth disease axonal type 2T
|
14866.0 |
|
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Aicardi-Goutieres syndrome
|
18866.0 |
|
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infantile osteopetrosis with neuroaxonal dysplasia
|
10866.0 |
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eustachian tube disease
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4866.0 |
|
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liver extraskeletal osteosarcoma
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3866.0 |
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bifid nose, autosomal recessive
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8866.0 |
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subpulmonary stenosis
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17866.0 |
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Bart-Pumphrey syndrome
|
7866.0 |
|
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hereditary spastic paraplegia 35
|
12866.0 |
|
