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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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corpus callosum agenesis-blepharophimosis-Robin sequence syndrome
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9021 |
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corpus callosum agenesis-neuronopathy syndrome
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902 |
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occipitotemporal lobe, and migraine with aura epilepsy
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C566902 |
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hereditary motor and sensory neuropathy with agenesis of the corpus callosum
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902 |
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brain stem angioblastoma
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3902 |
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glaucoma, open angle
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D005902 |
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secondary open angle glaucoma
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D005902 |
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optic neuritides, anterior
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D009902 |
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optic neuritis, anterior
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D009902 |
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congenital quadricuspid aortic valve
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D000082902 |
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peripheral neuropathy associated with agenesis of the corpus callosum
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902 |
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nerve injuries, auriculotemporal
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D000080902 |
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nerve injury, auriculotemporal
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D000080902 |
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osteopetrosis (disease), autosomal recessive
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19026 |
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adenoma, hepatocellular, benign
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18902 |
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