Paraparesis

Symptom Information:

Symptom ID: HPO:0002385
Synonyms:
Paraparesis [OMIM:Paraparesis]
Paraparesis [MedDRA:10033885]
Quality:
Cross references:
OMIM: "Paraparesis" [OMIM:Paraparesis]
UMLS:C0221166 "Paraparesis" [HPO:0002385]
Is a (Direct Parents):
HPO         Paraplegia/paraparesis
MedDRA Paralysis and paresis (excl cranial nerve)
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)
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)