Progressive gait ataxia

Symptom Information:

Symptom ID: HPO:0007240
Synonyms:
Gait ataxia, progressive [HPO:0007240]
Gait ataxia, progressive [OMIM:Gait ataxia, progressive]
Progressive gait ataxia [OMIM:Progressive gait ataxia]
Quality:
Cross references:
OMIM: "Gait ataxia, progressive" [OMIM:Gait ataxia, progressive]
OMIM: "Progressive gait ataxia" [OMIM:Progressive gait ataxia]
Is a (Direct Parents):
HPO         Gait ataxia
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 ataxia(HPO:0002066)
                      Progressive gait ataxia(HPO:0007240)
             Abnormality of central motor function(HPO:0011442)
                Abnormality of coordination(HPO:0011443)
                   Ataxia(HPO:0001251)
                      Gait ataxia(HPO:0002066)
                         Progressive gait ataxia(HPO:0007240)
MedDRA:
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)