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 | ||
|---|---|---|---|---|
| 26 |
 | Homocystinuria (Classic) | Text | |
| 27 |
 | Isobutyryl-CoA Dehydrogenase Deficiency | Text | |
| 28 |
 | Isovaleric Acidemia | Text | |
| 29 |
 | LCHAD and TFP Deficiency | Text | |
| 30 |
 | Malonic Acidemia | Text | |
| 31 |
 | Maple Syrup Urine Disease | Text | |
| 32 |
 | Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) | Text | |
| 33 |
 | Methylmalonic Acidemias | Text | |
| 34 |
 | Phenylketonuria (PKU) | Text | |
| 35 |
 | Pompe Disease | Text | |
| 36 |
 | Propionic Acidemia | Text | |
| 37 |
 | Pyruvate Carboxylase Deficiency | Text | |
| 38 |
 | Severe Combined Immunodeficiency (SCID) | Text | |
| 39 |
 | Short Chain Acyl-CoA Dehydrogenase Deficiency (SCADD) | Text | |
| 40 |
 | Sickle Cell Anemia | Text | |
| 41 |
 | Spinal Muscular Atrophy (SMA) | Text | |
| 42 |
 | Tyrosinemia Type 1 | Text | |
| 43 |
 | Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) | Text |