Oculomotor nerve palsy
Symptom Information:
Symptom ID: | HPO:0012246 | ||||
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 nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Abnormality of the cranial nerves(HPO:0001291) Oculomotor nerve palsy(HPO:0012246) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of eye movement(HPO:0000496) Ophthalmoparesis(HPO:0000597) Oculomotor nerve palsy(HPO:0012246) MedDRA: |
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Database Frequency: | 2 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |