Progressive spastic quadriplegia
Symptom Information:
Symptom ID: | HPO:0002478 | ||||
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) Hypertonia(HPO:0001276) Spasticity(HPO:0001257) Progressive spasticity(HPO:0002191) Progressive spastic quadriplegia(HPO:0002478) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Argininemia | (Orphanet:90) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
PELIZAEUS-MERZBACHER DISEASE | (OMIM:312080) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D | (OMIM:613811) |
Pseudoprogeria syndrome | (Orphanet:2985) |
Spondyloenchondrodysplasia | (Orphanet:1855) |