Abnormal conjugate eye movement
Symptom Information:
Symptom ID: | HPO:0000549 | ||
Synonyms: |
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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) Abnormal conjugate eye movement(HPO:0000549) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Spastic ataxia with congenital miosis | (Orphanet:1182) |