Progressive gait ataxia
Symptom Information:
Symptom ID: | HPO:0007240 | |||
Synonyms: |
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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 central motor function(HPO:0011442) Abnormality of coordination(HPO:0011443) Ataxia(HPO:0001251) Gait ataxia(HPO:0002066) Progressive gait ataxia(HPO:0007240) Abnormality of movement(HPO:0100022) Gait disturbance(HPO:0001288) Gait ataxia(HPO:0002066) Progressive gait ataxia(HPO:0007240) MedDRA: |
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Database Frequency: | 7 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Angelman syndrome | (Orphanet:72) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Spinocerebellar ataxia type 18 | (Orphanet:98771) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |