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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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primary (nonfamilial) amyloid neuropathies
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C531615 |
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autosomal dominant amyotrophic lateral sclerosis
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C531617 |
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isolated caroli disease
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C531647 |
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primary visual agnosia
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C531604 |
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congenital vocal cord paralysis
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15316 |
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skin type anthrax
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C531621 |
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familial lupus anticoagulant
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C531622 |
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familial spinal arachnoiditis
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C531624 |
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spinal tuberculous arachnoiditis
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C531624 |
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constricting bands, congenital
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C531614 |
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hb c disease
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C531699 |
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growth hormone excess
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C531600 |
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46,XX gonadal dysgenesis epibulbar dermoid
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C535316 |
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adult intracranial ependymoma
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C531673 |
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5 alpha fluorouracil toxicity
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C531667 |
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