Amme complex
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis | C1846242 | ACSL4 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 9598718, 11889465 | - |
| AMMECR1 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 10049589, 27811305 | - | ||
| KCNE5 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |