Lower limb hyperreflexia

Symptom Information:

Symptom ID: HPO:0002395
Synonyms:
Brisk lower extremity reflexes [HPO:0002395]
Hyperreflexia in lower limbs [HPO:0002395]
Hyperreflexia in the lower limbs [HPO:0002395]
Increased deep tendon reflexes in the lower limbs [HPO:0002395]
Leg hyperreflexia [HPO:0002395]
Brisk lower extremity reflexes [OMIM:Brisk lower extremity reflexes]
Hyperreflexia in lower limbs [OMIM:Hyperreflexia in lower limbs]
Hyperreflexia in the lower limbs [OMIM:Hyperreflexia in the lower limbs]
Increased deep tendon reflexes in the lower limbs [OMIM:Increased deep tendon reflexes in the lower limbs]
Leg hyperreflexia [OMIM:Leg hyperreflexia]
Lower limb hyperreflexia [OMIM:Lower limb hyperreflexia]
Lower limb hyperreflexia (reported in 1 patient) [OMIM:Lower limb hyperreflexia (reported in 1 patient)]
Quality:
Cross references:
OMIM: "Brisk lower extremity reflexes" [OMIM:Brisk lower extremity reflexes]
OMIM: "Hyperreflexia in lower limbs" [OMIM:Hyperreflexia in lower limbs]
OMIM: "Hyperreflexia in the lower limbs" [OMIM:Hyperreflexia in the lower limbs]
OMIM: "Increased deep tendon reflexes in the lower limbs" [OMIM:Increased deep tendon reflexes in the lower limbs]
OMIM: "Leg hyperreflexia" [OMIM:Leg hyperreflexia]
OMIM: "Lower limb hyperreflexia" [OMIM:Lower limb hyperreflexia]
OMIM: "Lower limb hyperreflexia (reported in 1 patient)" [OMIM:Lower limb hyperreflexia (reported in 1 patient)]
Is a (Direct Parents):
HPO         Hyperreflexia
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)
                   Hyperreflexia(HPO:0001347)
                      Lower limb hyperreflexia(HPO:0002395)
MedDRA:
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

ALZHEIMER DISEASE 3 (OMIM:607822)
Amish infantile epilepsy syndrome (Orphanet:171714)
Arnold-Chiari malformation type I (Orphanet:268882)
Autosomal dominant spastic paraplegia type 12 (Orphanet:100993)
Autosomal dominant spastic paraplegia type 13 (Orphanet:100994)
Autosomal dominant spastic paraplegia type 37 (Orphanet:171612)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 42 (Orphanet:171863)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal dominant striatal neurodegeneration (Orphanet:228169)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 27 (Orphanet:101007)
Autosomal recessive spastic paraplegia type 56 (Orphanet:320411)
Cerebroretinal vasculopathy (Orphanet:3421)
DPM1-CDG (Orphanet:79322)
Gaucher disease type 3 (Orphanet:77261)
HERNS syndrome (Orphanet:63261)
Hereditary vascular retinopathy (Orphanet:71291)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
Multiple sulfatase deficiency (Orphanet:585)
PELGER-HUET ANOMALY (OMIM:169400)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Spinocerebellar ataxia type 28 (Orphanet:101109)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
Syringomyelia (Orphanet:3280)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)