Disease

cone-rod dystrophy 16

Definition
A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22.
Synonyms
  • CORD16
  • retinal dystrophy with early macular involvement
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

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Associated Models