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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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congenital hereditary nonprogressive external ophthalmoplegia
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C563500 |
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GSD IV, nonprogressive hepatic
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C565540 |
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cerebellar hypoplasia, nonprogressive norman type
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C565865 |
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distal, congenital nonprogressive spinal muscular atrophy
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C563981 |
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myopathy, congenital nonprogressive with moebius and robin sequences
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C536102 |
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cerebellar disorder, nonprogressive, with mental retardation
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C535731 |
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myopathy, congenital nonprogressive, with moebius sequence and robin sequence
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C536102 |
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fetal status, nonreassuring
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D005316 |
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rhinitis, allergic, nonseasonal
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D012221 |
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dementia, familial nonspecific
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C579991 |
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hemolytic congenital, nonspherocytic anemia
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D000746 |
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hemolytic, congenital nonspherocytic anemia
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D000746 |
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anemia, congenital nonspherocytic hemolytic
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D000746 |
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lethal congenital nonspherocytic, with genital and other abnormalities hemolytic anemia
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C563935 |
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panniculitides, nodular nonsuppurative
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D010201 |
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