Unsteady gait
Symptom Information:
Symptom ID: | HPO:0002317 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |