Search Ontology:
Human Disease

X-linked cone-rod dystrophy 3

Term ID
DOID:0111007
Synonyms
  • CORDX3
Definition
A cone-rod dystrophy that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11. https://www.ncbi.nlm.nih.gov/pubmed/16505158
References
Ontology
Human Disease   ( DOID:0111007 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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