Search Ontology:
Human Disease

cone-rod dystrophy 11

Term ID
DOID:0111018
Synonyms
  • CORD11
Definition
A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the RAX2 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/25789692
References
Ontology
Human Disease   ( DOID:0111018 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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