The Medical Home Portal website was initiated in 2001 to improve the care of children with chronic conditions and special health care needs. In 2024 the content was archived by the Spencer S. Eccles Health Sciences Library in collaboration with the University of Utah's Department of Pediatrics.
| Title | Date | Type | ||
|---|---|---|---|---|
| 1 |
 | 2M3HBA Deficiency | Text | |
| 2 |
 | 3-Methylglutaconic Aciduria (3-MGA) | Text | |
| 3 |
 | 3MCC Deficiency | Text | |
| 4 |
 | Adrenoleukodystrophy (ALD) | Text | |
| 5 |
 | Argininemia | Text | |
| 6 |
 | Argininosuccinic Aciduria | Text | |
| 7 |
 | Beta-Ketothiolase Deficiency (BKD) | Text | |
| 8 |
 | Biotinidase Deficiency | Text | |
| 9 |
 | CACT and CPT II Deficiencies | Text | |
| 10 |
 | Carnitine Palmitoyltransferase 1A (CPT 1) Deficiency | Text | |
| 11 |
 | Carnitine Uptake Defect | Text | |
| 12 |
 | Citrullinemia Type 1 | Text | |
| 13 |
 | Citrullinemia Type 2 and Citrin Deficiency | Text | |
| 14 |
 | Congenital Adrenal Hyperplasia (CAH) | Text | |
| 15 |
 | Congenital Hypothyroidism | Text | |
| 16 |
 | Critical Congenital Heart Disease (CCHD) | Text | |
| 17 |
 | Cystic Fibrosis | Text | |
| 18 |
 | Fabry Disease | Text | |
| 19 |
 | Galactosemia | Text | |
| 20 |
 | Glutaric Acidemia Type 1 | Text | |
| 21 |
 | Glutaric Acidemia Type 2 | Text | |
| 22 |
 | Guanidinoacetate Methyltransferase (GAMT) Deficiency | Text | |
| 23 |
 | Hearing Loss and Deafness | Text | |
| 24 |
 | HMG-CoA Lyase Deficiency | Text | |
| 25 |
 | Holocarboxylase/Multiple Carboxylase Deficiency | Text |