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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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recessive mitochondrial ataxia syndrome
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19791 |
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autosomal dominant cerebellar ataxia type 3
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19793 |
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autosomal dominant cerebellar ataxia type 4
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19794 |
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autosomal dominant cerebellar ataxia type I
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19792 |
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autosomal dominant cerebellar ataxia type III
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19793 |
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autosomal dominant cerebellar ataxia type IV
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19794 |
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peripheral dysostosis-nasal hypoplasia-intellectual disability (PNM) syndrome
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19797 |
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nasal hypoplasia-peripheral dysostosis-intellectual disability syndrome
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19797 |
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obsolete acute hepatic porphyria
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19798.0 |
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adult-onset foveomacular dystrophy
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11979 |
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pseudo-vitelliform macular dystrophy
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11979 |
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adult-onset foveomacular dystrophy with choroidal neovascularization
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11979 |
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dumping (jejunal) syndrome
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1979 |
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adult-onset vitelliform macular dystrophy
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11979 |
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neuroleptic malignant syndrome
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19790 |
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