Unsteady gait

Symptom Information:

Symptom ID: HPO:0002317
Synonyms:
Gait instability [HPO:0002317]
Gait instability [OMIM:Gait instability]
Unsteady gait [OMIM:Unsteady gait]
Unstable gait [OMIM,du]
Quality:
Cross references:
OMIM: "Gait instability" [OMIM:Gait instability]
OMIM: "Unsteady gait" [OMIM:Unsteady gait]
Is a (Direct Parents):
HPO         Gait disturbance
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)
                   Unsteady gait(HPO:0002317)
MedDRA:
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-TELANGIECTASIA-LIKE DISORDER 2 (OMIM:615919)
Arnold-Chiari malformation type I (Orphanet:268882)
Ataxia - pancytopenia (Orphanet:2585)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
Autosomal recessive spastic paraplegia type 56 (Orphanet:320411)
Beta-mannosidosis (Orphanet:118)
CACH syndrome (Orphanet:135)
CEREBELLOPARENCHYMAL DISORDER II (OMIM:213100)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Congenital or early infantile CACH syndrome (Orphanet:157713)
Cree leukoencephalopathy (Orphanet:99854)
Developmental delay with autism spectrum disorder and gait instability (Orphanet:329195)
Fatal infantile lactic acidosis with methylmalonic aciduria (Orphanet:17)
Huntington disease-like 1 (Orphanet:157941)
Huntington disease-like 3 (Orphanet:157946)
Infantile neuroaxonal dystrophy (Orphanet:35069)
Juvenile or adult CACH syndrome (Orphanet:157719)
KURU, SUSCEPTIBILITY TO (OMIM:245300)
Late infantile CACH syndrome (Orphanet:157716)
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE (OMIM:300861)
MGAT2-CDG (Orphanet:79329)
Maternally-inherited diabetes and deafness (Orphanet:225)
Monosomy 22q13 (Orphanet:48652)
Myopathy due to myoadenylate deaminase deficiency (OMIM:615511)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A (OMIM:256600)
Non-progressive cerebellar ataxia with intellectual deficit (Orphanet:314647)
Ovarioleukodystrophy (Orphanet:99853)
PEROXISOME BIOGENESIS DISORDER 5B (OMIM:614867)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SPINOCEREBELLAR ATAXIA 37 (OMIM:615945)
SPINOCEREBELLAR ATAXIA 40 (OMIM:616053)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15 (OMIM:615705)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 (OMIM:615768)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17 (OMIM:616127)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
Syringomyelia (Orphanet:3280)
Triose phosphate-isomerase deficiency (Orphanet:868)
X-linked distal spinal muscular atrophy (Orphanet:139557)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)