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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
Hearing Impairment 96 (DFNB96) severe to profound hearing loss Autosomal Recessive 1p36.31-p36.13 0/Ansar et al., 2011
Hearing Impairment 89 (DFNB89) moderate-to severe hearing loss Autosomal Recessive 16q21-q23.2 0/Basit et al., 2011