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Details Of Syndromic Child Disease

Disease Name phenotype Inheritance Mode Chr Location Mutation Type Gene Name mRNA Variant Protein Variant Effect Reference
Bardet-Biedl Syndrome 15 Rod-cone dystrophy, learning difficulties, renal abnormalities, male hypogonadism, post-axial polydactyly, and obesity Autosomal Recessive 2p15 Substitution BBS15/WDPCP c.720C>A p.Cys240Ter Nonsense Nawaz et al., 2023/2023