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| language |
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| license |
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| created at |
2021-12-23 00:44:09 UTC |
| updated at |
2021-12-23 01:31:33 UTC |
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"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
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82,788 entries
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There is 0 pattern entry.
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brocq congenital, nonbullous form ichthyosiform erythroderma
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C538603 |
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uropathy distal obstructive polydactyly
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C536483 |
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ichthyosiform erythroderma, nonbullous, dominant form
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C537263 |
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gaucher disease, noncerebral juvenile
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D005776 |
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paragangliomas, familial nonchromaffin, 1
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D010236 |
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lymphoma, small noncleaved cell
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D008228 |
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lymphoma, small noncleaved-cell
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D008228 |
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autosomal dominant noncompaction of the left ventricular myocardium
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D056830 |
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x-linked isolated noncompaction of the left ventricular myocardium
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D056830 |
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left ventricular noncompaction with congenital heart defects
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C564690 |
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left ventricular noncompaction, isolated, autosomal dominant
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C565821 |
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left ventricular noncompaction, isolated, x-linked
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C564571 |
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left ventricular noncompaction, nonisolated
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C564690 |
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epilepsy, generalized nonconvulsive
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D004829 |
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seizure disorder, nonconvulsive generalized
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D004829 |
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