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| Vitamin metabolism disorders v2.0 | HLCS | Gene migrated from ENSG00000159267 to ENSG00000159267 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | HLCS |
Bryony Thompson gene: HLCS was added gene: HLCS was added to Vitamin metabolism disorders. Sources: Expert Review Green,ClinGen Mode of inheritance for gene: HLCS was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: HLCS were set to 10190325 Phenotypes for gene: HLCS were set to Disorders of biotin metabolism; holocarboxylase synthetase deficiency MONDO:0009666 |
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