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disease: EEM syndrome

id1142
nameEEM syndrome
variant-disease NM_001793.6(CDH3):c.1011G>C (p.Val337=) AND EEM syndrome
NM_001793.6(CDH3):c.1500C>T (p.Thr500=) AND EEM syndrome
NM_001793.6(CDH3):c.1240G>A (p.Ala414Thr) AND EEM syndrome
NM_001793.6(CDH3):c.2280+7C>T AND EEM syndrome
NM_001793.5(CDH3):c.-634_-633insG AND EEM syndrome
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