| Term Name: | Newfoundland cone-rod dystrophy |
|---|---|
| Synonyms: | NFRCD |
| Definition: | A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the RLBP1 gene on chromosome 15q26. |
| Ontology: | Human Disease [DOID:0111015] ( DOID:0111015 ) |