Paraplegia

Symptom Information:

Symptom ID: HPO:0010550
Synonyms:
Paraplegia [OMIM:Paraplegia]
Paraplegia [MedDRA:10033892]
Quality:
Cross references:
OMIM: "Paraplegia" [OMIM:Paraplegia]
UMLS:C0030486 "Paraplegia" [HPO:0010550]
Is a (Direct Parents):
HPO         Paraplegia/paraparesis
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)
                   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)
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)