OBO ID: DOID:0081023
Term Name: retinal cone dystrophy 4 Search Ontology:
Synonyms:
Definition: A cone dystrophy that has_material_basis_in homozygous mutation in the CACNA2D4 gene on chromosome 12p13. https://pubmed.ncbi.nlm.nih.gov/26560832/
References:
Ontology: Human Disease   ( DOID:0081023 )
OTHER retinal cone dystrophy 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNA2D4 Retinal cone dystrophy 4 610478
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None