FAHR Disease

TEST CODE MG08580
TEST NAME FAHR Disease
RELATED GENE SLC20A2
SYNONYMOUS SLC20A2
OMIM 213600
HEREDITY Autosomal Dominant
CLINICAL AREA FAHR Disease is an Autosomal Dominant inherited disease. Mutations in the SLC20A2 gene have been associated with the disease.
METHOD Next Generation Sequencing
SAMPLE TYPE Blood with EDTA
QUANTITY 3 ml
TAT 40 DAYS

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