Search Ontology:
Human Disease

cone-rod dystrophy 16

Term ID
DOID:0111022
Synonyms
  • CORD16
  • retinal dystrophy with early macular involvement
Definition
A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22. https://www.ncbi.nlm.nih.gov/pubmed/26865426
References
Ontology
Human Disease   ( DOID:0111022 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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