(Q32146175)
English
cone-rod dystrophy 16
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22
- CORD16
- retinal dystrophy with early macular involvement
- Retinitis Pigmentosa 64
- CONE-ROD DYSTROPHY 16; CORD16
- Cone-Rod Dystrophy type 16
- CONE-ROD DYSTROPHY 16
Statements
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference