| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011853 |
BXGD000752 |
Diabetes Mellitus, Experimental |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011884 |
BXGD000762 |
Diabetic Retinopathy |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0015397 |
BXGD000983 |
Disorder of eye |
Eye Diseases |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0028077 |
BXGD002069 |
Nyctalopia |
Eye Diseases |
| C0028738 |
BXGD002081 |
Nystagmus |
Eye Diseases; Nervous System Diseases |
| C0035334 |
BXGD002539 |
Retinitis Pigmentosa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0038379 |
BXGD002752 |
Strabismus |
Eye Diseases; Nervous System Diseases |
| C0234632 |
BXGD004691 |
Reduced visual acuity |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0271183 |
BXGD006169 |
Severe myopia |
Eye Diseases |
| C0339535 |
BXGD007263 |
Night blindness, congenital stationary |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0456909 |
BXGD008883 |
Blindness |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0494165 |
BXGD009022 |
Secondary malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0554970 |
BXGD009428 |
Pallor of optic disc |
|
| C0699791 |
BXGD009867 |
Stomach Carcinoma |
Digestive System Diseases; Neoplasms |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1298695 |
BXGD012251 |
Hypoplasia of optic disc |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases |
| C1848172 |
BXGD014908 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1850362 |
BXGD015134 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1854065 |
BXGD015379 |
LATE-ONSET RETINAL DEGENERATION (disorder) |
Eye Diseases |
| C1864870 |
BXGD016264 |
Night Blindness, Congenital Stationary, Autosomal Dominant 3 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1864877 |
BXGD016267 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1963184 |
BXGD016688 |
Nystagmus, CTCAE 3.0 |
|
| C3495587 |
BXGD018996 |
Night Blindness, Congenital Stationary, Type 1A |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C3501847 |
BXGD019030 |
Night blindness, congenital stationary, type 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C3551052 |
BXGD019144 |
Night blindness, stationary |
|
| C3669212 |
BXGD019325 |
Progressive retinal atrophy |
|
| C3711543 |
BXGD019396 |
X-Linked Csnb |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C4024756 |
BXGD021405 |
Abnormality of macular pigmentation |
|
| C4041558 |
BXGD021877 |
Cone-rod synaptic disorder, congenital nonprogressive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C4225345 |
BXGD022231 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G |
|
| C4551714 |
BXGD023398 |
Rod-Cone Dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C4554036 |
BXGD023557 |
Nystagmus, CTCAE 5.0 |
|