Lower limb hyperreflexia
Symptom Information:
Symptom ID: | HPO:0002395 | ||||||||||||
Synonyms: |
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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) Hyperreflexia(HPO:0001347) Lower limb hyperreflexia(HPO:0002395) MedDRA: |
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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) |