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| Miscellaneous Metabolic Disorders v0.318 | GCSH | Bryony Thompson Marked gene: GCSH as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Miscellaneous Metabolic Disorders v0.318 | GCSH | Bryony Thompson Gene: gcsh has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Miscellaneous Metabolic Disorders v0.318 | GCSH |
Bryony Thompson gene: GCSH was added gene: GCSH was added to Miscellaneous Metabolic Disorders. Sources: Literature Mode of inheritance for gene: GCSH was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: GCSH were set to 1671321; 27604308 Phenotypes for gene: GCSH were set to Glycine encephalopathy MIM#605899; Disorders of serine, glycine or glycerate metabolism Review for gene: GCSH was set to RED Added comment: Single case reported Sources: Literature |
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