Neuromuscular |
|
Brain and spinal cord malformations |
740.0–742.9 |
Mental retardation |
318.0–319.0 |
CNS degeneration and disease |
330.0–337.9 |
Infantile cerebral palsy |
343.0–343.9 |
Epilepsy |
345.0–345.9 |
Muscular dystrophies |
359.0–359.3 |
|
Cardiovascular |
|
Heart and great vessel malformations |
745.0–747.49 |
Cardiomyopathies |
425.0–425.4, 429.1 |
Conduction disorders and dysrhythmias |
426.0–427.4, 427.6–427.9 |
|
Respiratory |
|
Respiratory malformations |
748.0–748.9 |
Chronic respiratory disease Cystic fibrosis |
770.7 |
|
Renal |
|
Congenital anomalies |
753.0–753.9 |
Chronic renal failure |
585 |
|
Gastrointestinal |
|
Congenital anomalies |
750.3, 751.1–751.3, 751.6–751.9 |
Chronic liver disease and cirrhosis |
571.4–571.9 |
Inflammatory bowel disease |
550.556.9 |
|
Hematology and immunodeficiency |
|
Sickle-cell disease |
282.5–282.6 |
Hereditary anemias |
282.0–282.4 |
Hereditary immunodeficiency |
279.0–279.9, 288.1–288.2, 446.1 |
Human immunodeficiency virus |
42 |
|
Metabolic |
|
Amino acid metabolism |
270.0–270.9 |
Carbohydrate metabolism |
271.0–271.9 |
Lipid metabolism |
272.0–272.9 |
Storage disorders |
277.3, 277.5 |
Other metabolic disorders |
275.0–275.3, 277.2, 277.4, 277.6, 277.8–277.9 |
|
Other congenital or genetic defect |
|
Chromosomal anomalies |
758.0–758.9 |
Bone and joint anomalies |
259.4, 737.3, 756.0–756.5 |
Diaphragm and abdominal wall defects |
553.3, 756.6–756.7 |
Other congenital anomalies |
759.7 |
|
Malignancy |
|
Malignancy |
140.0–239.9 |
|
Cachexia and debility |
|
Cachexia |
799.4 |
Debility |
799.3 |