| C0009398 |
BXGD000604 |
Color vision defect |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0015310 |
BXGD000976 |
Exotropia |
Eye Diseases; Nervous System Diseases |
| C0015397 |
BXGD000983 |
Disorder of eye |
Eye Diseases |
| C0020490 |
BXGD001403 |
Hyperopia |
Eye Diseases |
| C0028738 |
BXGD002081 |
Nystagmus |
Eye Diseases; Nervous System Diseases |
| C0035309 |
BXGD002530 |
Retinal Diseases |
Eye Diseases |
| C0085636 |
BXGD003218 |
Photophobia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0152191 |
BXGD003556 |
Scotoma, Central |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0152200 |
BXGD003557 |
Achromatopsia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0234632 |
BXGD004691 |
Reduced visual acuity |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0236733 |
BXGD004822 |
Amphetamine-Related Disorders |
Chemically-Induced Disorders; Mental Disorders |
| C0236804 |
BXGD004835 |
Amphetamine Addiction |
Chemically-Induced Disorders; Mental Disorders |
| C0236807 |
BXGD004836 |
Amphetamine Abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0271092 |
BXGD006161 |
Progressive cone dystrophy (without rod involvement) |
Eye Diseases |
| C0271388 |
BXGD006196 |
Pendular Nystagmus |
Eye Diseases; Nervous System Diseases |
| C0302129 |
BXGD006830 |
Achromatopsia 1 |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0339526 |
BXGD007259 |
Autosomal recessive retinitis pigmentosa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0339537 |
BXGD007264 |
Cone monochromatism |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0374997 |
BXGD007967 |
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site |
|
| C0476397 |
BXGD008991 |
Electroretinogram abnormal |
|
| C0543968 |
BXGD009303 |
Cone dysfunction syndrome |
|
| C0730290 |
BXGD009946 |
Cone Dystrophy |
Eye Diseases |
| C0858618 |
BXGD011184 |
Dyschromatopsia |
|
| C0877008 |
BXGD011325 |
Enzyme inhibition disorder |
|
| C1288283 |
BXGD012175 |
Atrophoderma maculatum |
Skin and Connective Tissue Diseases |
| C1840457 |
BXGD014472 |
Retinal pigment epithelial atrophy |
|
| C1862475 |
BXGD016132 |
Abnormality of retinal pigmentation |
|
| C1963184 |
BXGD016688 |
Nystagmus, CTCAE 3.0 |
|
| C2673946 |
BXGD017234 |
Foveal hypoplasia (finding) |
|
| C2751308 |
BXGD017702 |
CONE DYSTROPHY 4 (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C2751309 |
BXGD017703 |
Achromatopsia 5 |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases |
| C3278975 |
BXGD018749 |
Attenuation of retinal blood vessels |
|
| C3665342 |
BXGD019277 |
Progressive Cone Dystrophy |
Eye Diseases |
| C3665347 |
BXGD019279 |
Visual Impairment |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C4024799 |
BXGD021424 |
Granular macular appearance |
|
| C4085590 |
BXGD022119 |
Cone-Rod Dystrophies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C4554036 |
BXGD023557 |
Nystagmus, CTCAE 5.0 |
|