Hypertelorism with midface prominence, myopia, mental retardation, and bone fragility
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility | C1970027 | IRX5 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 22581230 | - |