Search Ontology:
Human Disease

retinal cone dystrophy 4

Term ID
DOID:0081023
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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