Hemiparesis
Symptom Information:
| Symptom ID: | HPO:0001269 | ||||||||
| 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) Hemiplegia/hemiparesis(HPO:0004374) Hemiparesis(HPO:0001269) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Paralysis and paresis (excl cranial nerve)(MedDRA:10033800) Hemiparesis(HPO:0001269) |
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| Database Frequency: | 51 / 7739 | ||||||||
| Resource: |
All diseases associated with this symptom:
| 3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
| 3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
| Adult polyglucosan body disease | (Orphanet:206583) |
| Argininemia | (Orphanet:90) |
| Atypical hemolytic uremic syndrome | (Orphanet:2134) |
| Atypical hemolytic uremic syndrome with H factor anomaly | (Orphanet:93579) |
| Atypical hemolytic uremic syndrome with anti-factor H antibodies | (Orphanet:93581) |
| Bilateral frontal polymicrogyria | (Orphanet:208444) |
| CADASIL | (Orphanet:136) |
| CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS | (OMIM:601338) |
| Cardiofaciocutaneous syndrome | (Orphanet:1340) |
| Cerebroretinal vasculopathy | (Orphanet:3421) |
| Classical phenylketonuria | (Orphanet:79254) |
| Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
| Creutzfeldt-Jakob disease | (Orphanet:204) |
| Cystinosis | (Orphanet:213) |
| Encephalopathy due to GLUT1 deficiency | (Orphanet:71277) |
| Episodic ataxia type 6 | (Orphanet:209967) |
| Familial amyloid polyneuropathy | (Orphanet:85447) |
| Familial or sporadic hemiplegic migraine | (Orphanet:569) |
| Familial vascular leukoencephalopathy | (Orphanet:36383) |
| Gaucher disease | (Orphanet:355) |
| HERNS syndrome | (Orphanet:63261) |
| HHHH SYNDROME | (OMIM:306960) |
| Hereditary neurocutaneous angioma | (Orphanet:1062) |
| Hereditary vascular retinopathy | (Orphanet:71291) |
| Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
| Isolated focal cortical dysplasia type II | (Orphanet:268994) |
| Kearns-Sayre syndrome | (Orphanet:480) |
| Leber plus disease | (Orphanet:99718) |
| Leigh syndrome | (Orphanet:506) |
| MELAS | (Orphanet:550) |
| MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS | (OMIM:604317) |
| MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6 | (OMIM:607516) |
| MIGRAINE, FAMILIAL HEMIPLEGIC, 1 | (OMIM:141500) |
| MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
| MIGRAINE, FAMILIAL HEMIPLEGIC, 3 | (OMIM:609634) |
| MOYAMOYA DISEASE 6 WITH ACHALASIA | (OMIM:615750) |
| Maple syrup urine disease | (Orphanet:511) |
| Mitochondrial myopathy - lactic acidosis - deafness | (Orphanet:2597) |
| Monosomy 13q14 | (Orphanet:1587) |
| OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS | (OMIM:165200) |
| Pediatric systemic lupus erythematosus | (Orphanet:93552) |
| Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
| Progressive myoclonic epilepsy with dystonia | (Orphanet:352596) |
| Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
| Sinus node disease and myopia | (OMIM:182190) |
| Sneddon syndrome | (Orphanet:820) |
| Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |
| TERATOMA, PINEAL | (OMIM:273120) |
| Typical hemolytic uremic syndrome | (Orphanet:90038) |