OBO ID: DOID:0111007
Term Name: X-linked cone-rod dystrophy 3 Search Ontology:
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 X-linked cone-rod dystrophy 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNA1F Cone-rod dystrophy, X-linked, 3 300476
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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