Hecht syndrome
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Hecht syndrome (disorder) | C0265226 | MYH8 | Causal Pathogenic evidence from ClinVar | 8923935, 15282353, 17041932, 18049072, 20949528 | ClinVar |
| MYHAS | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |