Abnormality of refraction
Symptom Information:
| Symptom ID: | HPO:0000539 | ||||
| Synonyms: |
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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 refraction(HPO:0000539) MedDRA: |
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| Database Frequency: | 6 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Cardiofaciocutaneous syndrome | (Orphanet:1340) |
| Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
| Noonan syndrome | (Orphanet:648) |
| Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
| Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
| Williams syndrome | (Orphanet:904) |