Supranuclear gaze palsy

Symptom Information:

Symptom ID: HPO:0000605
Synonyms:
Supranuclear gaze paralysis [HPO:0000605]
Supranuclear gaze palsy [OMIM:Supranuclear gaze palsy]
Supranuclear gaze paralysis [OMIM:Supranuclear gaze paralysis]
Supranuclear gaze palsy (less common) [OMIM:Supranuclear gaze palsy (less common)]
Quality:
Cross references:
OMIM: "Supranuclear gaze palsy" [OMIM:Supranuclear gaze palsy]
OMIM: "Supranuclear gaze paralysis" [OMIM:Supranuclear gaze paralysis]
OMIM: "Supranuclear gaze palsy (less common)" [OMIM:Supranuclear gaze palsy (less common)]
Is a (Direct Parents):
HPO         Abnormality of eye movement
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:
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)