Spastic gait
Symptom Information:
Symptom ID: | HPO:0002064 | ||||
Synonyms: |
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Quality: | |||||
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) Abnormal pyramidal signs(HPO:0007256) Hypertonia(HPO:0001276) Spasticity(HPO:0001257) Spastic gait(HPO:0002064) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Paralysis and paresis (excl cranial nerve)(MedDRA:10033800) Spastic gait(HPO:0002064) |
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Database Frequency: | 46 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE | (OMIM:205100) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 12 | (Orphanet:100993) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 17 | (Orphanet:100998) |
Autosomal dominant spastic paraplegia type 19 | (Orphanet:100999) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal dominant spastic paraplegia type 36 | (Orphanet:320365) |
Autosomal dominant spastic paraplegia type 37 | (Orphanet:171612) |
Autosomal dominant spastic paraplegia type 38 | (Orphanet:171617) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 41 | (Orphanet:320355) |
Autosomal dominant spastic paraplegia type 42 | (Orphanet:171863) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 14 | (Orphanet:100995) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Autosomal recessive spastic paraplegia type 30 | (Orphanet:101010) |
Autosomal recessive spastic paraplegia type 32 | (Orphanet:171622) |
Autosomal recessive spastic paraplegia type 44 | (Orphanet:320401) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 49 | (Orphanet:320385) |
Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Episodic ataxia type 1 | (Orphanet:37612) |
Fucosidosis | (Orphanet:349) |
Hereditary continuous muscle fiber activity | (Orphanet:972) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked - psychosis - macroorchidism | (Orphanet:3077) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
Primary lateral sclerosis | (Orphanet:35689) |
SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE | (OMIM:615625) |
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |
Spastic paraplegia 33, autosomal dominant | (OMIM:610244) |
Spastic paraplegia type 2 | (Orphanet:99015) |
X-linked spastic paraplegia type 34 | (Orphanet:171607) |
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | (OMIM:607259) |