Spastic ataxia
Symptom Information:
Symptom ID: | HPO:0002497 | ||
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 central motor function(HPO:0011442) Abnormality of coordination(HPO:0011443) Ataxia(HPO:0001251) Spastic ataxia(HPO:0002497) MedDRA: |
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Database Frequency: | 13 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION | (OMIM:270500) |
Autosomal dominant spastic ataxia 1 | (Orphanet:251282) |
Autosomal recessive spastic ataxia - optic atrophy - dysarthria | (Orphanet:254343) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic ataxia with leukoencephalopathy | (Orphanet:314603) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Early-onset spastic ataxia-neuropathy syndrome | (Orphanet:313772) |
Methylcobalamin deficiency type cblDv1 | (Orphanet:308380) |
Methylmalonic acidemia with homocystinuria, type cblD | (Orphanet:79283) |
SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE | (OMIM:611302) |
Spastic ataxia - corneal dystrophy | (Orphanet:2572) |
Spastic ataxia with congenital miosis | (Orphanet:1182) |
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 | (Orphanet:308442) |