1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0111015 | Newfoundland cone-rod dystrophy | A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the RLBP1 gene on chromosome 15q26. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |