Abnormality of vision
Symptom Information:
| Symptom ID: | HPO:0000504 | ||||||
| Synonyms: |
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| Cross references: |
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| Is a (Direct Parents): |
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of vision(HPO:0000504) MedDRA: |
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| Database Frequency: | 22 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| 1p36 deletion syndrome | (Orphanet:1606) |
| Ataxia with vitamin E deficiency | (Orphanet:96) |
| Beta-thalassemia major | (Orphanet:231214) |
| Choroideremia | (Orphanet:180) |
| Cone rod dystrophy | (Orphanet:1872) |
| Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
| Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
| Disorder of bile acid synthesis | (Orphanet:79168) |
| Ectopia lentis - chorioretinal dystrophy - myopia | (Orphanet:1884) |
| Infantile Refsum disease | (Orphanet:772) |
| MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 | (OMIM:611638) |
| Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
| Night blindness - skeletal anomalies - dysmorphism | (Orphanet:1390) |
| Ocular albinism | (Orphanet:284804) |
| Osteochondrodysplatic nanism - deafness - retinitis pigmentosa | (Orphanet:2653) |
| Retinitis pigmentosa | (Orphanet:791) |
| Stern-Lubinsky-Durrie syndrome | (Orphanet:3194) |
| Usher syndrome | (Orphanet:886) |
| Usher syndrome type 1 | (Orphanet:231169) |
| Usher syndrome type 2 | (Orphanet:231178) |
| Usher syndrome type 3 | (Orphanet:231183) |
| X-linked immunoneurologic disorder | (Orphanet:2571) |