Paraparesis
Symptom Information:
Symptom ID: | HPO:0002385 | ||||
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) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Paralysis and paresis (excl cranial nerve)(MedDRA:10033800) Paraparesis(HPO:0002385) |
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Database Frequency: | 12 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Adrenomyeloneuropathy | (Orphanet:139399) |
Biotin-responsive basal ganglia disease | (Orphanet:65284) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 | (OMIM:105550) |
Frontotemporal dementia with motor neuron disease | (Orphanet:275872) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
NEUROFIBROMATOSIS, FAMILIAL SPINAL | (OMIM:162210) |
OCULODENTODIGITAL DYSPLASIA | (OMIM:164200) |
Oculodentodigital dysplasia | (Orphanet:2710) |
PAGET DISEASE OF BONE | (OMIM:602080) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |