Lower limb spasticity

Symptom Information:

Symptom ID: HPO:0002061
Synonyms:
Lower limb spasticity [OMIM:Lower limb spasticity]
Quality:
Cross references:
OMIM: "Lower limb spasticity" [OMIM:Lower limb spasticity]
Is a (Direct Parents):
HPO         Spasticity
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)
                         Lower limb spasticity(HPO:0002061)
MedDRA:
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

Adult polyglucosan body disease (Orphanet:206583)
Argininemia (Orphanet:90)
Arnold-Chiari malformation type I (Orphanet:268882)
Ataxia-telangiectasia-like disorder (Orphanet:251347)
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 29 (Orphanet:101009)
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 6 (Orphanet:100988)
Autosomal dominant spastic paraplegia type 8 (Orphanet:100989)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
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 18 (Orphanet:209951)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Autosomal recessive spastic paraplegia type 26 (Orphanet:101006)
Autosomal recessive spastic paraplegia type 27 (Orphanet:101007)
Autosomal recessive spastic paraplegia type 28 (Orphanet:101008)
Autosomal recessive spastic paraplegia type 30 (Orphanet:101010)
Autosomal recessive spastic paraplegia type 32 (Orphanet:171622)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
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 5A (Orphanet:100986)
Autosomal recessive spastic paraplegia type 7 (Orphanet:99013)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Hurler-Scheie syndrome (Orphanet:93476)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Juvenile amyotrophic lateral sclerosis (Orphanet:300605)
MASA syndrome (Orphanet:2466)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:260300)
Partington syndrome (Orphanet:94083)
Perrault Syndrome (Orphanet:2855)
Perrault Syndrome 3 (OMIM:614129)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION (OMIM:607565)
Spastic paraplegia 33, autosomal dominant (OMIM:610244)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
Spastic paraplegia type 2 (Orphanet:99015)
Syringomyelia (Orphanet:3280)
X-linked spastic paraplegia type 16 (Orphanet:100997)
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE (OMIM:607259)