Abnormality of saccadic eye movements
Symptom Information:
Symptom ID: | HPO:0000570 | |||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||
Quality: | ||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||
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) Abnormality of saccadic eye movements(HPO:0000570) MedDRA: Nervous system disorders(MedDRA:10029205) Cranial nerve disorders (excl neoplasms)(MedDRA:10011305) Abnormality of saccadic eye movements(HPO:0000570) Eye disorders(MedDRA:10015919) Ocular neuromuscular disorders(MedDRA:10030061) Ocular nerve and muscle disorders(MedDRA:10030059) Abnormality of saccadic eye movements(HPO:0000570) |
|||||||||||||||||||
Database Frequency: | 12 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Friedreich ataxia 1 | (OMIM:229300) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 3 | (Orphanet:77261) |
Huntington disease | (Orphanet:399) |
Infantile dystonia-parkinsonism | (Orphanet:238455) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome 1 | (OMIM:213300) |
Joubert syndrome 2 | (OMIM:608091) |
Leukoencephalopathy - dystonia - motor neuropathy | (Orphanet:163684) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |