Limited extraocular movements
Symptom Information:
Symptom ID: | HPO:0007941 | |||
Synonyms: |
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Quality: | ||||
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 morphology(HPO:0012372) Abnormality of the extraocular muscles(HPO:0008049) Limited extraocular movements(HPO:0007941) MedDRA: |
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Database Frequency: | 7 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Bilateral frontal polymicrogyria | (Orphanet:208444) |
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 1 | (OMIM:604377) |
Fatal infantile cytochrome C oxidase deficiency | (Orphanet:1561) |
Perrault Syndrome | (Orphanet:2855) |
Perrault Syndrome 1 | (OMIM:233400) |
Polymicrogyria due to TUBB2B mutation | (Orphanet:300573) |