Overview
Electroretinogram abnormal 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.
Ruvalcaba syndrome
Occasional (5-29%)
Bardet-Biedl syndrome
Frequent (30-79%)
Cockayne syndrome
Occasional (5-29%)
Retinitis pigmentosa
Very frequent (80-99%)
Retinitis pigmentosa-deafness syndrome
Very frequent (80-99%)
Leber's optic atrophy
Occasional (5-29%)
Choroideremia
Very frequent (80-99%)
Juvenile retinoschisis
Very frequent (80-99%)
Zellweger syndrome
Neurofibromatosis type 1
Occasional (5-29%)
Sorsby's fundus dystrophy
Leber's amaurosis
Frequent (30-79%)
Progressive cerebellar ataxia with hypogonadism
Very frequent (80-99%)
Proliferative vitreoretinopathy
Usher syndrome type 1
Very frequent (80-99%)
Usher syndrome type 2
Very frequent (80-99%)
Mitochondrial trifunctional protein deficiency
Frequent (30-79%)
Acyl-CoA oxidase deficiency
Very frequent (80-99%)
Acute zonal occult outer retinopathy
Occasional (5-29%)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy
Congenital fibrosis syndrome
Frequent (30-79%)
Deafness-dystonia syndrome
Distal arthrogryposis type 5
Frequent (30-79%)
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
Very frequent (80-99%)
Bothnia retinal dystrophy
Quick Facts
- SNOMED CT
- 274524001
- UMLS CUI
- C0476397
- Fully Specified Name
- Electroretinogram abnormal (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.