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| Rhabdomyolysis and Metabolic Myopathy v1.33 | SMDT1 | Zornitza Stark Marked gene: SMDT1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rhabdomyolysis and Metabolic Myopathy v1.33 | SMDT1 | Zornitza Stark Gene: smdt1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rhabdomyolysis and Metabolic Myopathy v1.33 | Zornitza Stark Copied gene SMDT1 from panel Mitochondrial disease | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rhabdomyolysis and Metabolic Myopathy v1.33 | SMDT1 |
Zornitza Stark gene: SMDT1 was added gene: SMDT1 was added to Rhabdomyolysis and Metabolic Myopathy. Sources: Expert Review Amber,Literature Mode of inheritance for gene: SMDT1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SMDT1 were set to 37454773 Phenotypes for gene: SMDT1 were set to Mitochondrial disease, MONDO:0044970, SMDT1-related |
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