Gait imbalance

Symptom Information:

Symptom ID: HPO:0002141
Synonyms:
Abnormality of balance [HPO:0002141]
Abnormality of equilibrium [HPO:0002141]
Dizziness [Orphanet:13620]
Dizziness and giddiness (finding) [Orphanet:13620]
Subjective vertigo (finding) [Orphanet:13620]
Giddiness (finding) [Orphanet:13620]
Dizziness (finding) [Orphanet:13620]
Dizziness and giddiness symptoms [Orphanet:13620]
Dysequilibrium [Orphanet:13620]
giddiness, vertigo [Orphanet:13620]
Gait imbalance [OMIM:Gait imbalance]
Giddiness [Orphanet:13620]
Dizziness [MedDRA:10013573]
Dizziness (excl vertigo) [MedDRA:10013573]
Dizziness and giddiness [MedDRA:10013573]
Dizzy [MedDRA:10013573]
Dizzy spells [MedDRA:10013573]
Faintness [MedDRA:10013573]
Felt faint [MedDRA:10013573]
Felt giddy [MedDRA:10013573]
Giddiness [MedDRA:10013573]
Light headedness [MedDRA:10013573]
Light-headed [MedDRA:10013573]
Light-headed feeling [MedDRA:10013573]
Lightheadedness [MedDRA:10013573]
Swaying feeling [MedDRA:10013573]
Wooziness [MedDRA:10013573]
Woozy [MedDRA:10013573]
Dizziness aggravated [MedDRA:10013573]
Balance disorder [MedDRA:10049848]
Balance difficulty [MedDRA:10049848]
Balance impaired NOS [MedDRA:10049848]
Disequilibrium syndrome [MedDRA:10049848]
Disorder equilibrium [MedDRA:10049848]
Dysequilibrium [MedDRA:10049848]
Equilibrium disorder of (NOS) [MedDRA:10049848]
Unsteadiness [MedDRA:10049848]
Equilibrium loss [MedDRA:10049848]
Equilibrium trouble [MedDRA:10049848]
Impairment of balance (finding) [Orphanet:43210]
Problem with balance (finding) [Orphanet:43210]
Equilibration disorder [Orphanet:43210]
Dysequilibrium [Orphanet:43210]
Ataxia/incoordination/trouble of the equilibrium [Orphanet:43210]
Quality:
Cross references:
HPO:0002321 "Vertigo" [Orphanet:13620]
Orphanet:13620 "Dizziness" [Orphanet:13620]
Orphanet:43210 "Ataxia/incoordination/trouble of the equilibrium" [Orphanet:43210]
OMIM: "Gait imbalance" [OMIM:Gait imbalance]
UMLS:C0476206 "Dizziness and giddiness symptoms" [Orphanet:13620]
UMLS:C0281825 "Dysequilibrium" [Orphanet:13620]
UMLS:C0012833 "Dizziness" [Orphanet:13620]
UMLS:C0476207 "giddiness, vertigo" [Orphanet:13620]
UMLS:C0575090 "Equilibration disorder" [Orphanet:43210]
UMLS:C0281825 "Dysequilibrium" [Orphanet:43210]
Is a (Direct Parents):
Orphanet Functional anomalies of the inner ear
Orphanet Ataxia
HPO         Gait disturbance
MedDRA Coordination and balance disturbances
Orphanet [DEL]Motor deficit/trouble
MedDRA Neurological signs and symptoms NEC
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)
       Neurological signs and symptoms NEC(MedDRA:10029306)
          Gait imbalance(HPO:0002141)
       Coordination and balance disturbances(MedDRA:10072984)
          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)