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 |