| Metadata | |
|---|---|
| ID | DOID:0110333 |
| Name | Leber congenital amaurosis 7 |
| Definition | A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/9537410 |
| Xrefs | |
| Synonyms |
LCA7 [EXACT] |
| Parent Relationships |
is_a Leber congenital amaurosis is_a monogenic disease |
| Subclass Logical Relationships |
disease has basis in some gene disease has basis in some Abnormality of prenatal development or birth |