| Disease ID | Source | Name | Description |
| 602531 | OMIM | Grange syndrome (GRNG) | An autosomal recessive syndrome of stenosis or occlusion of multiple arteries, including renal, abdominal, cerebral and probably coronary arteries, congenital heart defects, brachydactyly, syndactyly, bone fragility, and learning disabilities. The disease is caused by variants affecting the gene represented in this entry. |