16 Del. Admin. Code § 4101-6.0
Current through Register Vol. 28, No. 7, January 1, 2025
In the event any particular clause or section of the regulations should be declared invalid or unconstitutional by any court of competent jurisdiction, the remaining portions shall remain in full force and effective.
Table 1: APPENDIX A October 2002
| DELAWARE BIRTH DEFECTS REGISTRY REPORTABLE DIAGNOSES | ||
| Broad Categories | Specific Categories | ICD-9 Codes |
| Congenital Infections | ||
| Congenital syphilis | 090.0 - 090.3 | |
| Congenital rubella | 771.0 | |
| Congenital cytomegalovirus | 771.1 | |
| Congenital toxoplasmosis (not specific code) | 771.2 | |
| Other infections specific to perinatal period | 771.80 | |
| Other congenital infections | 771.x | |
| Neoplasms | Neurofibromatosis | 237.70 |
| Endocrine, Nutritional, Metabolic, Immunological Diseases | ||
| Congenital hypothyroidism | 243.00 | |
| Phenylketonuria | 270.10 | |
| Galactosemia | 271.1 | |
| Cystic Fibrosis | 277.00.01 | |
| Other Metabolic diseases | ||
| Diseases of Blood | ||
| Sickle Cell Disease | 282.60 | |
| Other hemoglobinopathies | 282.63, 282.69, 282.4 | |
| Developmental Disorders | ||
| Developmental Language Disorder | 315.31-315.39 | |
| Coordination Disorder | 315.40 | |
| Mental Retardation | 317 - 319 | |
| Congenital Anomalies of Central Nervous System | ||
| Anencephalus | 740.0 -740.1 | |
| Spina bifida without anencephalus | 741.0,741.9 w/o 740.0-740.10 | |
| Hydrocephalus without spina bifida | 742.3 w/o 741.0, 741.9 | |
| Encephalocele | 742.0 | |
| Microcephalus | 742.1 | |
| Holoprosencephaly/Porencephaly | 742.2 | |
| Other Congenital Anomalies of Nervous System | 742.4 - 742.9 | |
| Congenital Anomalies of the Eye | ||
| Anophthalmia/microphthalmia | 743.0,743.1 | |
| Congenital cataract | 743.30 -743.34 | |
| Aniridia | 743.45 | |
| Glaucoma | 743.20 -743.22 | |
| Coloboma | 743.46* | |
| Congenital Anomalies of the Ear | ||
| Anotia/microtia | 744.01,744.23 | |
| Congenital Anomalies of the Cardiovascular System | ||
| Common truncus | 745.0 | |
| Transposition of great arteries | 745.10,745.11, 745.12, 745.19 | |
| Tetralogy of Fallot | 745.2 | |
| Ventricular septal defect | 745.4 | |
| Atrial Septal Defect | 745.5 | |
| Endocardial cushion defect | 745.60,745.61, 745.69 | |
| Single Ventricle | 745.3 | |
| Pulmonary valve atresia and stenosis | 746.01,746.02 | |
| Tricuspid valve atresia and stenosis | 746.1 | |
| Ebstein's anomaly | 746.2 | |
| Aortic valve stenosis | 746.3 | |
| Hypoplastic left heart syndrome | 746.7 | |
| Patent ductus arteriosus >2500 gms | 747.0 | |
| Coarctation of aorta | 747.10 | |
| Pulmonary artery anomalies | 747.3 | |
| Congenital anomalies of the Respiratory System | ||
| Anomalies of larynx/trachea/bronchus | 748.30 | |
| Lung agenesis/hypoplasia | 748.5 | |
| Other respiratory anomalies | ||
| Congenital Anomalies of the Orofacial Area | ||
| Cleft palate without cleft lip | 749.00 -749.04 | |
| Cleft lip with or without cleft palate | 749.1,749.2 | |
| Choanal atresia | 748.0 | |
| Congenital Anomalies of the Gastrointestinal Tract | ||
| Esophageal atresia/tracheoesophageal fistula | 750.3 | |
| Atresia/stenosis of intestine and rectum | 751.10,751.2 | |
| Hirschsprung's disease (congenital megacolon) | 751.3 | |
| Anomalies of internal fixation of bowel | 751.40 | |
| Biliary atresia | 751.61 | |
| Malrotation of intestine | 751.4* | |
| Pyloric stenosis | 750.5 | |
| Anorectal malformation | 751.4* | |
| Congenital Anomalies of the Genitourinary System | ||
| Renal Agenesis/hypoplasia | 753.0 | |
| Bladder exstrophy | 753.5 | |
| Cloacal exstrophy | * | |
| Cystic/dysplastic kidneys | 753.10,753.15 | |
| Obstructive genitourinary defect | 753.2,753.6 | |
| Hypospadias and Epispadias | 752.6 | |
| Ambiguous genitalia | 752.9* | |
| Polycystic kidneys | 753.12 -753.14 | |
| Congenital Anomalies of the Musculoskeletal Regions | ||
| Reduction defect, upper limbs | 755.20 -755.29 | |
| Polydactyly/ Syndactyly/ Adactyly | 755.00 -755.02 755.10 -755.14 755.4* | |
| Reduction defect, lower limbs | 755.30-755.39 | |
| Arthrogryposis multiplex congenital | 754.89* | |
| Achondroplasia | 756.4 | |
| Osteogenesis imperfecta | 756.51 | |
| Other skeletal dysplasia Gastroschisis | 756.7 | |
| Omphalocele | 756.7 | |
| Diaphragmatic hernia (moved up) | 756.6 | |
| Scoliosis/Lordosis/Kyphosis | 754.0, 756.19 | |
| Congenital hip dysplasia | 754.30, 754.31 | |
| 754.35* | ||
| Club Foot | 754.50, 51, 53, 60, 70, 79 | |
| Craniosynostosis | 756.0* | |
| Chromosomal Disorders | ||
| Trisomy 21 (Down syndrome) | 758.0 | |
| Trisomy 13 | 758.1 | |
| Trisomy 18 | 758.2 | |
| Autosomal deletion syndromes | 758.30 | |
| Other conditions due to autosomal anomalies | 758.50 | |
| Gonadal dysgenesis (Turner's syndrome) | 758.60 | |
| Klinefelter's syndrome | 758.70 | |
| Other conditions due to sex chromosome anomalies | 758.80 | |
| Conditions due to anomaly of unspecified Chromosome | 758.90 | |
| Fragile X Syndrome | 759.83 | |
| Other Congenital Malformations | ||
| Amniotic bank disruption complex | no code | |
| Embryopathy from Toxic Exposure in Utero | ||
| Fetal Alcohol syndrome | 760.71 | |
| Phenytoin | 760.79* | |
| Isotretinoin | 760.79* | |
| Warfarin | 760.79* | |
| Other toxic exposures | 760.7x | |
| Conductive hearing loss, external ear | 389.01 | |
| Conductive hearing loss, middle ear | 389.03 | |
| Ear disorder, unspecified | 388.9 | |
| Hearing loss, noise-induced | 388.12 | |
| Hearing loss, sudden, unspecified | 388.2 | |
| Hearing loss, unspecified | 388.9 | |
| Sensorineural hearing loss, unspecified | 389.10 | |
16 Del. Admin. Code § 4101-6.0