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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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autosomal dominant parkinson disease 3
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C566552 |
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hypospadias, and penoscrotal inversion anal atresia
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C566526 |
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TNF Receptor-associated periodic syndrome (TRAPS)
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C536657 |
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polymicrogyria, bilateral perisylvian
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C536658 |
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congenital bilateral perisylvian syndrome
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C536658 |
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hereditary adult-onset painful axonal polyneuropathy
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14665 |
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coal miner's pneumoconiosis
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6654 |
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coal workers' pneumoconiosis
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6654 |
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myopia, and sensorineural deafness spondyloepiphyseal dysplasia
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C566659 |
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cataracts, cleft palate, and mental retardation spondyloepiphyseal dysplasia with coronal craniosynostosis
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C566515 |
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Bell's (facial) palsy
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5665 |
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facial nerve palsy
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5665 |
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hidrotic, autosomal recessive ectodermal dysplasia
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C566553 |
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congenital, autosomal recessive fibrosis of extraocular muscles
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C566587 |
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congenital bilateral recurrent nerve paralysis and ptosis
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8665 |
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