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Details Of NON Syndromic Child Disease

Disease Name phenotype Inheritance Mode Chr Location Mutation Type Gene Name mRNA Variant Protein Variant Effect Reference
Hereditary congenital cataract 3 (HCC3,EPHA2) Cataract 3 Autosomal Recessive 1p36.13 Deletion EPHA2 c.2710delG p.Val904Cysfs*36 Frameshift Jarwar et al., 2021/2021