Progressive spastic paraparesis
Symptom Information:
Symptom ID: | HPO:0007199 | ||
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) Paraparesis(HPO:0002385) Spastic paraparesis(HPO:0002313) Progressive spastic paraparesis(HPO:0007199) Hypertonia(HPO:0001276) Spasticity(HPO:0001257) Lower limb spasticity(HPO:0002061) Spastic paraparesis(HPO:0002313) Progressive spastic paraparesis(HPO:0007199) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Adult polyglucosan body disease | (Orphanet:206583) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |