Spastic gait

Symptom Information:

Symptom ID: HPO:0002064
Synonyms:
Spastic gait [OMIM:Spastic gait]
Gait spastic [MedDRA:10017585]
Quality:
Cross references:
OMIM: "Spastic gait" [OMIM:Spastic gait]
Is a (Direct Parents):
HPO         Spasticity
MedDRA Paralysis and paresis (excl cranial nerve)
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)
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)