Eyelid apraxia
Symptom Information:
Symptom ID: | HPO:0000658 | ||||
Synonyms: |
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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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Apraxia(HPO:0002186) Eyelid apraxia(HPO:0000658) Abnormality of central motor function(HPO:0011442) Apraxia(HPO:0002186) Eyelid apraxia(HPO:0000658) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) Eyelid apraxia(HPO:0000658) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyelid(HPO:0000492) Eyelid apraxia(HPO:0000658) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Classical progressive supranuclear palsy | (Orphanet:240071) |
PARKINSON DISEASE 20, EARLY-ONSET | (OMIM:615530) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |