Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
medical condition
|
| gptkbp:affects |
both sexes
|
| gptkbp:alsoKnownAs |
achromatopsia
|
| gptkbp:cause |
genetic disorder
cone cell dysfunction |
| gptkbp:diagnosedBy |
electroretinography
color vision test |
| gptkbp:firstDescribed |
19th century
|
| https://www.w3.org/2000/01/rdf-schema#label |
total color blindness
|
| gptkbp:ICD-10_code |
H53.5
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:MeSH_ID |
D003118
|
| gptkbp:OMIM |
216900
|
| gptkbp:prevalence |
rare
|
| gptkbp:relatedTo |
color blindness
|
| gptkbp:symptom |
nystagmus
photophobia inability to perceive color poor visual acuity |
| gptkbp:treatment |
visual aids
tinted lenses |
| gptkbp:bfsParent |
gptkb:Color_blindness
|
| gptkbp:bfsLayer |
7
|