Hemiplegia

Symptom Information:

Symptom ID: HPO:0002301
Synonyms:
Hemiplegia (disorder) [Orphanet:43370]
Hemiplegia [Orphanet:43370]
Hemiplegia [OMIM:Hemiplegia]
Hemiplegia/diplegia/hemiparesia/limb palsy [Orphanet:43370]
Hemiplegia [MedDRA:10019468]
Flaccid hemiplegia [MedDRA:10019468]
Hemiplegia (left) [MedDRA:10019468]
Hemiplegia (right) [MedDRA:10019468]
Hemiplegia crossed [MedDRA:10019468]
Hemiplegia transient [MedDRA:10019468]
Hemiplegia, unspecified [MedDRA:10019468]
Left hemiplegia [MedDRA:10019468]
Left sided paralysis [MedDRA:10019468]
Other specified hemiplegia [MedDRA:10019468]
Paralysis one side of body [MedDRA:10019468]
Right hemiplegia [MedDRA:10019468]
Right sided paralysis [MedDRA:10019468]
Spastic hemiplegia [MedDRA:10019468]
Hemiplegia (rare) [OMIM:Hemiplegia (rare)]
Diplegia [MedDRA:10013033]
Diplegia (disorder) [Orphanet:43370]
Diplegia [Orphanet:43370]
Diplegia [OMIM:Diplegia]
Quality:
Cross references:
HPO:0004374 "Hemiplegia/hemiparesis" [Orphanet:43370]
Orphanet:43370 "Hemiplegia/diplegia/hemiparesia/limb palsy" [Orphanet:43370]
OMIM: "Hemiplegia" [OMIM:Hemiplegia]
OMIM: "Hemiplegia (rare)" [OMIM:Hemiplegia (rare)]
OMIM: "Diplegia" [OMIM:Diplegia]
UMLS:C0018991 "Hemiplegia" [HPO:0002301]
UMLS:C0018991 "Hemiplegia" [Orphanet:43370]
UMLS:C0221165 "Diplegia" [Orphanet:43370]
Is a (Direct Parents):
Orphanet [DEL]Motor deficit/trouble
HPO         Hemiplegia/hemiparesis
Orphanet Hemiparesis
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)
                      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)
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)