Paralysis

Symptom Information:

Symptom ID: HPO:0003470
Synonyms:
Paralysis [OMIM:Paralysis]
Paralysis [MedDRA:10033799]
Quality:
Cross references:
OMIM: "Paralysis" [OMIM:Paralysis]
UMLS:C0522224 "Paralysis" [HPO:0003470]
Is a (Direct Parents):
MedDRA Paralysis and paresis (excl cranial nerve)
HPO         Abnormality of central motor function
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)
                Paralysis(HPO:0003470)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Paralysis and paresis (excl cranial nerve)(MedDRA:10033800)
          Paralysis(HPO:0003470)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Acute intermittent porphyria (Orphanet:79276)
Alpers syndrome (Orphanet:726)
Autosomal dominant spastic paraplegia type 10 (Orphanet:100991)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
CEREBRAL CAVERNOUS MALFORMATIONS 3 (OMIM:603285)
Encephalopathy due to GLUT1 deficiency (Orphanet:71277)
GM2-gangliosidosis, AB variant (Orphanet:309246)
Gitelman syndrome (Orphanet:358)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Progressive demyelinating neuropathy with bilateral striatal necrosis (Orphanet:217396)
Self-healing collodion baby (Orphanet:281122)