Table: screening_disorders_by_race_ethnicity
race_ethnicity disorder_type disorder_count screened_count rate_per_100_000
American Indian Cystic fibrosis (CF) 9 52784 17.05
American Indian Hypothyroidism, primary congenital (PCH) 25 52784 47.36
American Indian Sickle Cell Disease 8 52784 15.16
Asian Indian Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 10 124895 8.01
Asian Indian Congenital adrenal hyperplasia, classical salt wasting (CAH) 6 124895 4.80
Asian Indian Cystic fibrosis (CF) 9 124895 7.21
Asian Indian Hypothyroidism, primary congenital (PCH) 119 124895 95.28
Asian Indian Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 7 124895 5.60
Black 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 6 417395 1.44
Black ALD - not otherwise specified 9 146183 6.16
Black ALD carrier (female) 10 146183 6.84
Black Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 6 417395 1.44
Black Congenital adrenal hyperplasia, classical salt wasting (CAH) 10 417395 2.40
Black Cystic fibrosis (CF) 26 417395 6.23
Black Hypothyroidism, primary congenital (PCH) 71 417395 17.01
Black Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 8 417395 1.92
Black Phenylketonuria (PKU) 11 417395 2.64
Black Sickle Cell Disease 809 417395 193.82
Black Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) 8 417395 1.92
Chinese, Japanese, Korean 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 8 347140 2.30
Chinese, Japanese, Korean ALD carrier (female) 8 140973 5.67
Chinese, Japanese, Korean Congenital adrenal hyperplasia, classical salt wasting (CAH) 16 347140 4.61
Chinese, Japanese, Korean Hypothyroidism, primary congenital (PCH) 173 347140 49.84
Chinese, Japanese, Korean Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 8 347140 2.30
Chinese, Japanese, Korean Phenylketonuria (PKU) 15 347140 4.32
Filipino, Laotian, Vietnamese, Cambodian, Other Southeast Asian Hypothyroidism, primary congenital (PCH) 105 256588 40.92
Filipino, Laotian, Vietnamese, Cambodian, Other Southeast Asian Phenylketonuria (PKU) 8 256588 3.12
Hawaiian, Guamanian, Samoan Hypothyroidism, primary congenital (PCH) 7 12988 53.90
Hispanic 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 93 2593521 3.59
Hispanic ALD - not otherwise specified 43 855678 5.03
Hispanic ALD carrier (female) 50 855678 5.84
Hispanic Argininosuccinyl-CoA lyase deficiency (ASAL deficiency) 8 2593521 0.31
Hispanic Biotinidase deficiency profound (BD) 43 2593521 1.66
Hispanic Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 22 2593521 0.85
Hispanic Citrullinemia type I (argininosuccinic acid synthetase deficiency (ASAS deficiency)/CIT-1) 16 2593521 0.62
Hispanic Congenital adrenal hyperplasia, classical salt wasting (CAH) 131 2593521 5.05
Hispanic Congenital adrenal hyperplasia, classical simple virilizing (CAH) 15 2593521 0.58
Hispanic Cystic fibrosis (CF) 249 2593521 9.60
Hispanic Galactosemia, classical 23 2593521 0.89
Hispanic Glutaric acidemia type I (GA1) 25 2593521 0.96
Hispanic Hypothyroidism, primary congenital (PCH) 1570 2593521 60.54
Hispanic Isovaleric acidemia (IVA) 18 2593521 0.69
Hispanic Maple syrup urine disease (MSUD) 14 2593521 0.54
Hispanic Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 105 2593521 4.05
Hispanic Methylmalonic acidemia mut 0 (MMA) 13 2593521 0.50
Hispanic Methylmalonic acidemia mut- (MMA) 6 2593521 0.23
Hispanic Phenylketonuria (PKU) 71 2593521 2.74
Hispanic Pompe - late onset Pompe disease 6 303942 1.97
Hispanic Propionic acidemia (PA) 12 2593521 0.46
Hispanic SCID, severe combined immunodeficiency 25 1540969 1.62
Hispanic Sickle Cell Disease 64 2593521 2.47
Hispanic Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) 19 2593521 0.73
Middle Eastern Hypothyroidism, primary congenital (PCH) 30 75195 39.90
Middle Eastern Phenylketonuria (PKU) 10 75195 13.30
Other 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 7 97996 7.14
Other Cystic fibrosis (CF) 8 97996 8.16
Other Hypothyroidism, primary congenital (PCH) 50 97996 51.02
Other Sickle Cell Disease 21 97996 21.43
White 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 17 1321415 1.29
White ALD - not otherwise specified 20 436495 4.58
White ALD carrier (female) 20 436495 4.58
White Biotinidase deficiency profound (BD) 21 1321415 1.59
White Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 21 1321415 1.59
White Congenital adrenal hyperplasia, classical salt wasting (CAH) 48 1321415 3.63
White Congenital adrenal hyperplasia, classical simple virilizing (CAH) 6 1321415 0.45
White Cystic fibrosis (CF) 305 1321415 23.08
White Galactosemia, classical 26 1321415 1.97
White Glutaric acidemia type I (GA1) 13 1321415 0.98
White Hypothyroidism, primary congenital (PCH) 510 1321415 38.59
White Isovaleric acidemia (IVA) 13 1321415 0.98
White Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 111 1321415 8.40
White Phenylketonuria (PKU) 100 1321415 7.57
White SCID, severe combined immunodeficiency 14 795061 1.76
White Sickle Cell Disease 8 1321415 0.61
White Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) 10 1321415 0.76