Hemiplegia
Symptom Information:
Symptom ID: | HPO:0002301 | |||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) Hemiplegia(HPO:0002301) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Paralysis and paresis (excl cranial nerve)(MedDRA:10033800) Hemiplegia(HPO:0002301) |
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Database Frequency: | 42 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 | (OMIM:614820) |
Adult polyglucosan body disease | (Orphanet:206583) |
Argininemia | (Orphanet:90) |
Autosomal recessive hyper-IgE syndrome | (Orphanet:169446) |
CADASIL | (Orphanet:136) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Classical phenylketonuria | (Orphanet:79254) |
Coats plus syndrome | (Orphanet:313838) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
Episodic ataxia type 6 | (Orphanet:209967) |
Fabry disease | (Orphanet:324) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Gaucher disease | (Orphanet:355) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
HERNS syndrome | (Orphanet:63261) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hurler syndrome | (Orphanet:93473) |
Isolated sulfite oxidase deficiency | (Orphanet:99731) |
Kearns-Sayre syndrome | (Orphanet:480) |
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS | (OMIM:614561) |
MELAS | (Orphanet:550) |
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) |
Maple syrup urine disease | (Orphanet:511) |
Monosomy 13q14 | (Orphanet:1587) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PORENCEPHALY 1 | (OMIM:175780) |
PORENCEPHALY 2 | (OMIM:614483) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Porencephaly | (Orphanet:2940) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Sinus node disease and myopia | (OMIM:182190) |
Sneddon syndrome | (Orphanet:820) |
X-linked reticulate pigmentary disorder with systemic manifestations | (Orphanet:85453) |