Section 115.04. Congenital and metabolic disorders.

  Pursuant to s. 253.13 (1) , Stats., each newborn shall be tested for all of the following conditions:

(1)  

(a) Phenylketonuria (PKU), ICD-10-CM-E70.0.

(b) Hyperphenylalaninemia, ICD-10-CM-E70.1

(2)  Galactosemia, ICD-10-CM-E74.21 .

(3)  Congenital hypothyroidism, ICD-10-CM-E03.1 .

(4)  Hemoglobinopathies, including all of the following:

(a) Sickle cell disease, ICD-10-CM-D57.1.

(b) Hemoglobin S-beta Thalassemia, ICD-10-CM-D57.40.

(c) Hemoglobin SC disease, ICD-10-CM-D57.20.

(d) Hemoglobin disease other, ICD-10-CM-D58.2.

(5)  Biotinidase deficiency, ICD-10-CM-D81.810.

(6)  Congenital adrenal hyperplasia, ICD-10-CM-E25.0.

(7)  Cystic fibrosis, ICD-10-CM-E84.9.

(8)  Fatty acid oxidation disorders, including all of the following:

(a) Medium-chain acyl-CoA dehydrogenase deficiency, ICD-10-CM-E71.311.

(b) Long-chain L-3-Hydroxy acyl-CoA dehydrogenase deficiency, ICD-10-CM-E71.318.

(c) Very long-chain acyl-CoA dehydrogenase deficiency, ICD-10-CM-E71.310.

(d) Carnitine palmitoyltransferase II deficiency, ICD-10-CM-E71.318.

(e) Carnitine-acylcarnitine translocase deficiency, ICD-10-CM-E71.318.

(f) Glutaric acidemia type II, ICD-10-CM-E71.313.

(g) 2, 4-Dienoyl-CoA reductase deficiency, ICD-10-CM-E71.318.

(h) Carnitine uptake defect, ICD-10-CM-E71.41.

(i) Medium/short-chain hydroxy CoA dehydrogenase deficiency, ICD-10-CM-E71.318.

(j) Medium-chain ketoacyl-CoA thiolase deficiency, ICD-10-CM-E71.318.

(9)  Maple Syrup Urine Disease, ICD-10-CM-E71.0.

(10)  Homocystinuria, ICD-10-CM-E72.11.

(11)  Tyrosinemia types I, II, and III, ICD-10-CM-E70.21.

(12)  Citrullinemia types I and II, ICD-10-CM-E72.23.

(13)  Argininosuccinic acidura, ICD-10-CM-E72.22.

(14)  Severe Combined Immunodeficiency and related conditions of immunodeficiency, ICD-10-CM-D81.9.

(15)  Organic acidemias, including all of the following:

(a) Glutaric acidemia type I, ICD-10-CM-E72.3.

(b) Propionic acidemia, ICD-10-CM-E71.121.

(c) Methylmalonic acidemia (CBL A, B, C, D; MUT), ICD-10-CM-E71.120.

(d) Isovaleric acidemia, ICD-10-CM-E71.110.

(e) 3-Methylcrotony1-CoA carboxylase deficiency, ICD-10-CM-E71.19.

(f) Multiple carboxylase deficiency, ICD-10-CM-D81.818.

(g) 3-Methylglutaconic aciduria, ICD-10-CM-E71.111.

(h) beta-Ketothiolase deficiency, ICD-10-CM-E71.19.

(i) 2-Methyl-3-hydroxbutyric aciduria, ICD-10-CM-
E71.19.

(j) 3-Hydroxy-3-methylglutaric aciduria, ICD-10-CM-
E71.118.

(16)  Critical congenital heart disease, including all of the following:

(a)

1. Coarctation of the aorta, ICD-10-CM-Q25.1.

2. Atresia of aorta, ICD-10-CM-Q25.2.

3. Stenosis of aorta, ICD-10-CM-Q25.3.

(b)

1. Double outlet right ventricle, ICD-10-CM-Q20.1.

2. Double outlet left ventricle, ICD-10-CM-Q20.2.

(c) Ebstein's anomaly, ICD-10-CM-Q22.5.

(d)

1. Hypoplastic left heart syndrome ICD-10-CM-Q23.4.

2. Congenital mitral stenosis or atresia, ICD-10-CM-Q23.2.

(e)

1. Interrupted aortic arch, ICD-10-CM-Q25.4.

2. Atresia of aorta, ICD-10-CM-Q25.2.

3. Stenosis of aorta, ICD-10-CM-Q25.3.

(f)

1. Pulmonary valve atresia, ICD-10-CM-Q22.0.

2. Other congenital malformations of the pulmonary valve, ICD-10-CM-Q22.3.

3. Atresia of pulmonary artery, ICD-10-CM-Q25.5.

(g) Single ventricle heart disease variants other than HLHS, including all of the following:

1. Hypoplastic right heart syndrome, ICD-10-CM-Q22.6.

2. Other congenital malformations of the tricuspid valve ICD-10-CM-Q22.8.

3. Congenital malformations of the tricuspid valve unspecified, ICD-10-CM-Q22.9.

4. Double inlet ventricle, ICD-10-CM-Q20.4.

(h) Tetralogy of fallot, ICD-10-CM-Q21.3.

(i)

1. Total anomalous pulmonary venous return, ICD-10-CM-Q26.2.

2. Anomalous pulmonary venous connection, unspecified, ICD-10-CM-Q26.4.

3. Partial anomalous pulmonary venous connection, ICD-10-CM-Q26.3.

(j) Transposition of the great vessels, ICD-10-CM-Q20.3.

(k) Tricuspid atresia and stenosis, ICD-10-CM-Q22.4.

(L) Truncus arteriosus, ICD-10-CM-Q20.0.

Cr. Register, May, 1993, No. 449 , eff. 6-1-93; emerg. am. (5) and (6), cr. (7), eff. 1-31-95; correction in (intro.) made under s. 13.93 (2m) (b) 7., Stats., Register, July, 1995, No. 475 ; am. (5) and (6), cr. (7), Register, July, 1995, No. 475 , eff. 8-1-95; am. (intro.) and (1) to (6), cr. (8), Register, December, 1999, No. 528 , eff. 1-1-00; emerg. cr. (9) to (13), eff. 10-12-02; CR 02-136 : cr. (9) to (13) Register March 2003 No. 567 , eff. 4-1-03; emerg. cr. (14), eff. 1-1-08; CR 08-005 : cr. (14) Register June 2008 No. 630 , eff. 7-1-08; CR 14-074 : am. (intro.), cr. (15), (16) Register July 2015 No. 715 , eff. 8-1-15, and renum. (1) to (1) (a) and am., cr. (1) (b), am. (2), (3), r. and recr. (4), am. (5) to (7), r. and recr. (8), am. (9) to (14), r. and recr. (15), am. (16) Register July 2015 No. 715 , eff. 10-1-15; correction in (15) (g) made under s. 35.17, Stats., Register September 2015 No. 717 .