|OBO ID: DOID:13911|
|Term Name:||achromatopsia||Search Ontology:|
|Definition:||A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. (4)|
|Ontology:||Human Disease (DOID:13911)|
OTHER achromatopsia PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.