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Disease Ontology Term: achromatopsia

DO ID
DOID:13911
Description
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.
Synonyms
ACHM, Monochromatism
View DO Annotations for yeast and other model organisms at the Alliance of Genome Resources

Ontology Diagram

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Annotations

Manually Curated

There are no manually curated annotations for achromatopsia.

High-throughput

There are no high-throughput annotations for achromatopsia.

Computational

There are no computational annotations for achromatopsia.