RS368440234 MYH9
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Associated Conditions
MYH9-related disorder
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Inborn genetic diseases
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
MYH9-related disorder
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Inborn genetic diseases
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
Other Variants in MYH9