Paraplegia
Symptom Information:
Symptom ID: | HPO:0010550 | ||||
Synonyms: |
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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) Weakness due to upper motor neuron dysfunction(HPO:0010549) Paraplegia/paraparesis(HPO:0010551) Paraplegia(HPO:0010550) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Paralysis and paresis (excl cranial nerve)(MedDRA:10033800) Paraplegia(HPO:0010550) |
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Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ATTRV122I amyloidosis | (Orphanet:85451) |
Arachnoid cyst | (Orphanet:2356) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
Familial amyloid polyneuropathy | (Orphanet:85447) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Leber plus disease | (Orphanet:99718) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |