| Metadata | |
|---|---|
| ID | DOID:0061178 |
| Name | autosomal recessive congenital nystagmus 8 |
| Definition | A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2. https://pubmed.ncbi.nlm.nih.gov/35348658/ |
| Xrefs | |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal inheritance disease has basis in some Abnormality of prenatal development or birth |