Table: screening_disorders_by_california_region
california_region disease_type case_count number_screened percent_of_all_disorders_in_region
Central Coast 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 19 557240 3
Central Coast ALD - not otherwise specified 11 185798 2
Central Coast ALD carrier (female) 18 185798 3
Central Coast Biotinidase deficiency profound (BD) 7 557240 1
Central Coast Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 10 557240 2
Central Coast Congenital adrenal hyperplasia, classical salt wasting (CAH) 27 557240 4
Central Coast Cystic fibrosis (CF) 81 557240 13
Central Coast Galactosemia, classical 6 557240 1
Central Coast Hypothyroidism, primary congenital (PCH) 334 557240 55
Central Coast Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 29 557240 5
Central Coast Phenylketonuria (PKU) 31 557240 5
Central Coast Sickle Cell Disease 22 557240 4
Central Coast Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) 7 557240 1
Los Angeles 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 30 1372349 2
Los Angeles ALD - not otherwise specified 28 446768 2
Los Angeles ALD carrier (female) 25 446768 2
Los Angeles Biotinidase deficiency profound (BD) 26 1372349 2
Los Angeles Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 16 1372349 1
Los Angeles Citrullinemia type I (argininosuccinic acid synthetase deficiency (ASAS deficiency)/CIT-1) 6 1372349 <1
Los Angeles Congenital adrenal hyperplasia, classical salt wasting (CAH) 72 1372349 5
Los Angeles Congenital adrenal hyperplasia, classical simple virilizing (CAH) 9 1372349 1
Los Angeles Cystic fibrosis (CF) 111 1372349 7
Los Angeles Galactosemia, classical 13 1372349 1
Los Angeles Glutaric acidemia type I (GA1) 6 1372349 <1
Los Angeles Hypothyroidism, primary congenital (PCH) 720 1372349 46
Los Angeles Isovaleric acidemia (IVA) 13 1372349 1
Los Angeles Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 44 1372349 3
Los Angeles Methylmalonic acidemia mut 0 (MMA) 6 1372349 <1
Los Angeles Phenylketonuria (PKU) 62 1372349 4
Los Angeles SCID, severe combined immunodeficiency 10 818577 1
Los Angeles Sickle Cell Disease 339 1372349 22
Los Angeles Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) 13 1372349 1
Northern Central Valley 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 9 600705 1
Northern Central Valley ALD - not otherwise specified 7 208611 1
Northern Central Valley ALD carrier (female) 13 208611 2
Northern Central Valley Biotinidase deficiency profound (BD) 6 600705 1
Northern Central Valley Congenital adrenal hyperplasia, classical salt wasting (CAH) 19 600705 3
Northern Central Valley Cystic fibrosis (CF) 94 600705 14
Northern Central Valley Galactosemia, classical 9 600705 1
Northern Central Valley Glutaric acidemia type I (GA1) 15 600705 2
Northern Central Valley Hypothyroidism, primary congenital (PCH) 293 600705 43
Northern Central Valley Isovaleric acidemia (IVA) 7 600705 1
Northern Central Valley Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 34 600705 5
Northern Central Valley Methylmalonic acidemia mut- (MMA) 6 600705 1
Northern Central Valley Phenylketonuria (PKU) 31 600705 5
Northern Central Valley SCID, severe combined immunodeficiency 10 368154 1
Northern Central Valley Sickle Cell Disease 126 600705 18
Northern Central Valley Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) 7 600705 1
Northern, Mountain, and Desert Areas 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 15 531584 3
Northern, Mountain, and Desert Areas ALD - not otherwise specified 6 181961 1
Northern, Mountain, and Desert Areas ALD carrier (female) 11 181961 2
Northern, Mountain, and Desert Areas Biotinidase deficiency profound (BD) 10 531584 2
Northern, Mountain, and Desert Areas Congenital adrenal hyperplasia, classical salt wasting (CAH) 17 531584 3
Northern, Mountain, and Desert Areas Cystic fibrosis (CF) 110 531584 19
Northern, Mountain, and Desert Areas Galactosemia, classical 9 531584 2
Northern, Mountain, and Desert Areas Glutaric acidemia type I (GA1) 11 531584 2
Northern, Mountain, and Desert Areas Hypothyroidism, primary congenital (PCH) 265 531584 47
Northern, Mountain, and Desert Areas Isovaleric acidemia (IVA) 6 531584 1
Northern, Mountain, and Desert Areas Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 35 531584 6
Northern, Mountain, and Desert Areas Phenylketonuria (PKU) 36 531584 6
Northern, Mountain, and Desert Areas Sickle Cell Disease 35 531584 6
San Francisco Bay Area 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 18 569659 3
San Francisco Bay Area ALD - not otherwise specified 11 198146 2
San Francisco Bay Area ALD carrier (female) 13 198146 2
San Francisco Bay Area Biotinidase deficiency profound (BD) 12 569659 2
San Francisco Bay Area Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 15 569659 3
San Francisco Bay Area Congenital adrenal hyperplasia, classical salt wasting (CAH) 35 569659 6
San Francisco Bay Area Cystic fibrosis (CF) 61 569659 10
San Francisco Bay Area Galactosemia, classical 12 569659 2
San Francisco Bay Area Hypothyroidism, primary congenital (PCH) 233 569659 39
San Francisco Bay Area Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 30 569659 5
San Francisco Bay Area Phenylketonuria (PKU) 31 569659 5
San Francisco Bay Area Sickle Cell Disease 119 569659 20
Southern Coast 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 32 849368 4
Southern Coast ALD - not otherwise specified 14 300351 2
Southern Coast ALD carrier (female) 13 300351 2
Southern Coast Biotinidase deficiency profound (BD) 8 849368 1
Southern Coast Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 12 849368 1
Southern Coast Citrullinemia type I (argininosuccinic acid synthetase deficiency (ASAS deficiency)/CIT-1) 10 849368 1
Southern Coast Congenital adrenal hyperplasia, classical salt wasting (CAH) 26 849368 3
Southern Coast Cystic fibrosis (CF) 116 849368 14
Southern Coast Glutaric acidemia type I (GA1) 6 849368 1
Southern Coast Hypothyroidism, primary congenital (PCH) 426 849368 51
Southern Coast Isovaleric acidemia (IVA) 8 849368 1
Southern Coast Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 40 849368 5
Southern Coast Phenylketonuria (PKU) 38 849368 5
Southern Coast SCID, severe combined immunodeficiency 6 525211 1
Southern Coast Sickle Cell Disease 75 849368 9
Southern Inland Empire 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency) 22 832462 2
Southern Inland Empire ALD - not otherwise specified 11 287941 1
Southern Inland Empire Biotinidase deficiency profound (BD) 8 832462 1
Southern Inland Empire Carnitine transporter deficiency (CTD)/carnitine uptake defect (CUD) 12 832462 1
Southern Inland Empire Citrullinemia type I (argininosuccinic acid synthetase deficiency (ASAS deficiency)/CIT-1) 7 832462 1
Southern Inland Empire Congenital adrenal hyperplasia, classical salt wasting (CAH) 37 832462 4
Southern Inland Empire Cystic fibrosis (CF) 119 832462 12
Southern Inland Empire Glutaric acidemia type I (GA1) 7 832462 1
Southern Inland Empire Hypothyroidism, primary congenital (PCH) 418 832462 44
Southern Inland Empire Medium chain acyl-CoA dehydrogenase deficiency (MCAD Deficiency) 42 832462 4
Southern Inland Empire Phenylketonuria (PKU) 55 832462 6
Southern Inland Empire SCID, severe combined immunodeficiency 11 510607 1
Southern Inland Empire Sickle Cell Disease 196 832462 21
Southern Inland Empire Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) 11 832462 1