Search Ontology:
Human Disease

cone-rod dystrophy 24

Term ID
DOID:0081449
Synonyms
Definition
A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11. https://pubmed.ncbi.nlm.nih.gov/35947183/
References
Ontology
Human Disease   ( DOID:0081449 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models