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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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MME-related autosomal dominant Charcot Marie Tooth disease type 2
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44657 |
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MME-related autosomal dominant hereditary motor and sensory neuropathy type 2
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44657 |
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alzheimer disease, familial, 10
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C566465 |
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disease or disorder of skull
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24654 |
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sella turcica, empty
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D004652 |
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sella turcicas, empty
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D004652 |
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pleural, tuberculous empyema
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D004654 |
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early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome
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44651 |
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epidermolytic verrucous epidermal nevus
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44656 |
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primary ciliary dyskinesia 30
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14465 |
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primary ciliary dyskinesia 30 without situs inversus
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14465 |
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primary ciliary dyskinesia 32
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14657 |
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primary ciliary dyskinesia 32 without situs inversus
|
14657 |
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primary ciliary dyskinesia caused by mutation in CCDC151
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14465 |
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primary ciliary dyskinesia caused by mutation in RSPH3
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14657 |
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