Internuclear ophthalmoplegia
Symptom Information:
| Symptom ID: | HPO:0030773 | ||
| Synonyms: |
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| Quality: | deprecated | ||
| Cross references: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of eye movement(HPO:0000496) Ophthalmoparesis(HPO:0000597) Ophthalmoplegia(HPO:0000602) Internuclear ophthalmoplegia(HPO:0030773) MedDRA: |
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| Database Frequency: | 2 / 7739 | ||
| Resource: | HPO |
All diseases associated with this symptom:
| Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
| Sneddon syndrome | (Orphanet:820) |