Spastic ataxia

Symptom Information:

Symptom ID: HPO:0002497
Synonyms:
Spastic ataxia [OMIM:Spastic ataxia]
Quality:
Cross references:
OMIM: "Spastic ataxia" [OMIM:Spastic ataxia]
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)
                      Spastic ataxia(HPO:0002497)
MedDRA:
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)