Overview
Abnormal color vision is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Bardet-Biedl syndrome
Frequent (30-79%)
Retinitis pigmentosa
Occasional (5-29%)
Hypogonadotropic hypogonadism
Occasional (5-29%)
Fundus flavimaculatus
Very frequent (80-99%)
Tritan defect
Achromatopsia
Very frequent (80-99%)
Leber's optic atrophy
Occasional (5-29%)
Stargardt's disease
Very frequent (80-99%)
Choroideremia
Occasional (5-29%)
Tritanopia
Hypogonadism with anosmia
Occasional (5-29%)
Sjogren-Larsson syndrome
Frequent (30-79%)
Hereditary sensory and motor neuropathy, type VI
ABL - Abetalipoproteinaemia
Frequent (30-79%)
Adult vitelliform macular dystrophy
Frequent (30-79%)
Usher syndrome type 2
Occasional (5-29%)
Congenital stationary night blindness
Very rare (1-4%)
Bietti's crystalline retinopathy
Occasional (5-29%)
Progressive bulbar palsy with sensorineural deafness
Occasional (5-29%)
Deafness-dystonia syndrome
Occasional (5-29%)
Jalili syndrome
Very frequent (80-99%)
Autosomal dominant vitreoretinochoroidopathy
Young onset Parkinson disease
Occasional (5-29%)
Benson syndrome
Frequent (30-79%)
Bothnia retinal dystrophy
Very frequent (80-99%)
Related Symptoms
Quick Facts
- SNOMED CT
- 23289000
- UMLS CUI
- C0234629
- Fully Specified Name
- Abnormal color vision (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.