Search Ontology:
Human Disease

cone-rod dystrophy 13

Term ID
DOID:0111016
Synonyms
  • CORD13
Definition
A cone-rod dystrophy that has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.2. https://www.ncbi.nlm.nih.gov/pubmed/12920076
References
Ontology
Human Disease   ( DOID:0111016 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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