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| Disease_Term | Source | Rank | Other Values | CAP myopathy 2, 609285 (3) | OMIM | high |
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Nemaline myopathy 4, autosomal dominant, 609285 (3) | OMIM | high |
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Arthrogryposis multiplex congenita, distal, type 1, 108120 (3) | OMIM | high |
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Arthrogryposis, distal, type 2B, 601680 (3) | OMIM | high |
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