Supranuclear gaze palsy
Symptom Information:
Symptom ID: | HPO:0000605 | ||||
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 eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of eye movement(HPO:0000496) Supranuclear gaze palsy(HPO:0000605) MedDRA: |
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Database Frequency: | 16 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
Autosomal dominant spastic ataxia 1 | (Orphanet:251282) |
Classical progressive supranuclear palsy | (Orphanet:240071) |
Creutzfeldt-Jakob disease | (Orphanet:204) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 | (OMIM:105550) |
Frontotemporal dementia with motor neuron disease | (Orphanet:275872) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
PARKINSON DISEASE 20, EARLY-ONSET | (OMIM:615530) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |