RS140662138 MYH9
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Associated Conditions
Glomerulonephritis
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Autosomal dominant nonsyndromic hearing loss 17
Inborn genetic diseases
Glomerulonephritis
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Autosomal dominant nonsyndromic hearing loss 17
Inborn genetic diseases
Other Variants in MYH9