| Disease ID | Source | Name | Description |
| 618884 | OMIM | Proteinuria, chronic benign (PROCHOB) | An autosomal recessive condition characterized by isolated, non-progressive proteinuria in absence of renal disease and hypertension. Onset of proteinuria is in the first decade of life. The disease is caused by variants affecting the gene represented in this entry. |
| 261100 | OMIM | Imerslund-Grasbeck syndrome 1 (IGS1) | A form of Imerslund-Grasbeck syndrome, a rare autosomal recessive disorder characterized by vitamin B12 deficiency commonly resulting in megaloblastic anemia, which is responsive to parenteral vitamin B12 therapy and appears in infancy or early childhood. Clinical manifestations include failure to thrive, infections and neurological damage. Mild proteinuria, with no signs of kidney disease, is present in about half of the patients. The disease is caused by variants affecting the gene represented in this entry. |