Progressive cerebellar ataxia

Symptom Information:

Symptom ID: HPO:0002073
Synonyms:
Cerebellar ataxia, progressive [HPO:0002073]
Progressive ataxia [HPO:0002073]
Cerebellar ataxia, progressive [OMIM:Cerebellar ataxia, progressive]
Progressive cerebellar ataxia [OMIM:Progressive cerebellar ataxia]
Ataxia, progressive [OMIM:Ataxia, progressive]
Progressive ataxia (onset second year of life) [OMIM:Progressive ataxia (onset second year of life)]
Quality:
Cross references:
OMIM: "Cerebellar ataxia, progressive" [OMIM:Cerebellar ataxia, progressive]
OMIM: "Progressive cerebellar ataxia" [OMIM:Progressive cerebellar ataxia]
OMIM: "Ataxia, progressive" [OMIM:Ataxia, progressive]
OMIM: "Progressive ataxia (onset second year of life)" [OMIM:Progressive ataxia (onset second year of life)]
Is a (Direct Parents):
HPO         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 central motor function(HPO:0011442)
                Abnormality of coordination(HPO:0011443)
                   Ataxia(HPO:0001251)
                      Progressive cerebellar ataxia(HPO:0002073)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant spastic paraplegia type 10 (Orphanet:100991)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Bangstad syndrome (Orphanet:1227)
Behr syndrome (Orphanet:1239)
CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA (OMIM:212890)
DYSTONIA WITH CEREBELLAR ATROPHY (OMIM:611694)
Familial paroxysmal ataxia (Orphanet:97)
Gaucher disease type 3 (Orphanet:77261)
LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY (OMIM:606183)
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation (Orphanet:137898)
Mevalonic aciduria (Orphanet:29)
Perrault Syndrome 5 (OMIM:616138)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 10 (Orphanet:98761)
Spinocerebellar ataxia type 11 (Orphanet:98767)
Spinocerebellar ataxia type 12 (Orphanet:98762)
Spinocerebellar ataxia type 13 (Orphanet:98768)
Spinocerebellar ataxia type 14 (Orphanet:98763)
Spinocerebellar ataxia type 19/22 (Orphanet:98772)
Spinocerebellar ataxia type 2 (Orphanet:98756)
Spinocerebellar ataxia type 21 (Orphanet:98773)
Spinocerebellar ataxia type 3 (Orphanet:98757)
Spinocerebellar ataxia type 4 (Orphanet:98765)
Spinocerebellar ataxia type 6 (Orphanet:98758)
Spinocerebellar ataxia type 7 (Orphanet:94147)
Spinocerebellar ataxia type 8 (Orphanet:98760)