×

Details Of NON Syndromic Child Disease

Disease Name phenotype Inheritance Mode Chr Location Mutation Type Gene Name mRNA Variant Protein Variant Effect Reference
Tooth Agenesis,Oligodontia (MSX1) oligodontia and tooth anamolies Autosomal Recessive 4p16.1?p16.3 Missense MSX1 655G>A Ala219Thr Amino Acid Substitution 0/Chishti et al., 2006