Gait imbalance
Symptom Information:
Symptom ID: | HPO:0002141 | ||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||||||||||||||||||||
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 movement(HPO:0100022) Gait disturbance(HPO:0001288) Gait imbalance(HPO:0002141) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Coordination and balance disturbances(MedDRA:10072984) Gait imbalance(HPO:0002141) Neurological signs and symptoms NEC(MedDRA:10029306) Gait imbalance(HPO:0002141) |
||||||||||||||||||||||||||||||||||||||||||||
Database Frequency: | 55 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
48,XXYY syndrome | (Orphanet:10) |
Aceruloplasminemia | (Orphanet:48818) |
Alpha-N-acetylgalactosaminidase deficiency | (Orphanet:3137) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Argininosuccinic aciduria | (Orphanet:23) |
Bangstad syndrome | (Orphanet:1227) |
Bardet-Biedl syndrome | (Orphanet:110) |
Behçet disease | (Orphanet:117) |
Catecholaminergic polymorphic ventricular tachycardia | (Orphanet:3286) |
Classical progressive supranuclear palsy | (Orphanet:240071) |
Cogan syndrome | (Orphanet:1467) |
Crigler-Najjar syndrome | (Orphanet:205) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Deafness - oligodontia | (Orphanet:3230) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Fabry disease | (Orphanet:324) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Familial thrombocytosis | (Orphanet:71493) |
Giant cell arteritis | (Orphanet:397) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
HERNS syndrome | (Orphanet:63261) |
Hydatidosis | (Orphanet:400) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Kearns-Sayre syndrome | (Orphanet:480) |
Lassa fever | (Orphanet:99824) |
Leigh syndrome | (Orphanet:506) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
Malignant atrophic papulosis | (Orphanet:679) |
Maple syrup urine disease | (Orphanet:511) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Multiple sclerosis - ichthyosis - factor VIII deficiency | (Orphanet:3151) |
Naxos disease | (Orphanet:34217) |
Neurofibromatosis type 2 | (Orphanet:637) |
Niemann-Pick disease type C | (Orphanet:646) |
Nipah virus disease | (Orphanet:99825) |
Pendred syndrome | (Orphanet:705) |
Polycythemia vera | (Orphanet:729) |
Primary familial polycythemia | (Orphanet:90042) |
Pulmonary arterial hypertension | (Orphanet:182090) |
Relapsing polychondritis | (Orphanet:728) |
Rift valley fever | (Orphanet:319251) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
Sneddon syndrome | (Orphanet:820) |
TRAPS syndrome | (Orphanet:32960) |
Tyrosinemia type 2 | (Orphanet:28378) |
VERTIGO, BENIGN RECURRENT | (OMIM:193007) |
Waldenström macroglobulinemia | (Orphanet:33226) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolfram syndrome | (Orphanet:3463) |