Paralysis
Symptom Information:
Symptom ID: | HPO:0003470 | ||||
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) 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) |
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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) |