Hemiplegia/hemiparesis

Symptom Information:

Symptom ID: HPO:0004374
Synonyms:
Hemiplegia [Orphanet:43370]
Hemiparesia [Orphanet:43370]
Hemiplegia (disorder) [Orphanet:43370]
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:0002301 "Hemiplegia" [Orphanet:43370]
HPO:0001269 "Hemiparesis" [Orphanet:43370]
Orphanet:43370 "Hemiplegia/diplegia/hemiparesia/limb palsy" [Orphanet:43370]
OMIM: "Hemiplegia (rare)" [OMIM:Hemiplegia (rare)]
OMIM: "Diplegia" [OMIM:Diplegia]
UMLS:C0018991 "Hemiplegia" [Orphanet:43370]
UMLS:C0221165 "Diplegia" [Orphanet:43370]
Is a (Direct Parents):
MedDRA Paralysis and paresis (excl cranial nerve)
HPO         Weakness due to upper motor neuron dysfunction
Orphanet [DEL]Motor deficit/trouble
Orphanet Hemiparesis
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)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Paralysis and paresis (excl cranial nerve)(MedDRA:10033800)
          Hemiplegia/hemiparesis(HPO:0004374)
Database Frequency: 158 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3-methylglutaconic aciduria type 1 (Orphanet:67046)
3-methylglutaconic aciduria type 3 (Orphanet:67047)
Acute intermittent porphyria (Orphanet:79276)
Adams-Oliver syndrome (Orphanet:974)
Adult familial nephronophtisis - spastic quadriparesia (Orphanet:2666)
Adult polyglucosan body disease (Orphanet:206583)
Aicardi syndrome (Orphanet:50)
Aicardi-Goutières syndrome (Orphanet:51)
Alexander disease (Orphanet:58)
Alpers syndrome (Orphanet:726)
Alpha-N-acetylgalactosaminidase deficiency (Orphanet:3137)
Alpha-N-acetylgalactosaminidase deficiency type 1 (Orphanet:79279)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alveolar echinococcosis (Orphanet:284)
Apolipoprotein A-I deficiency (Orphanet:425)
Argininemia (Orphanet:90)
Arterial dissection - lentiginosis (Orphanet:1682)
Ataxia with vitamin E deficiency (Orphanet:96)
Atypical Rett syndrome (Orphanet:3095)
Atypical teratoid tumor (Orphanet:99966)
Behçet disease (Orphanet:117)
CADASIL (Orphanet:136)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Cerebellar ataxia - hypogonadism (Orphanet:1173)
Cerebro-reno-digital syndrome (Orphanet:1396)
Cerebroretinal vasculopathy (Orphanet:3421)
Charcot-Marie-Tooth disease (Orphanet:166)
Classical homocystinuria (Orphanet:394)
Classical phenylketonuria (Orphanet:79254)
Cobb syndrome (Orphanet:53721)
Cogan syndrome (Orphanet:1467)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Congenital ichthyosis - microcephalus - tetraplegia (Orphanet:2271)
Corneal-cerebellar syndrome (Orphanet:3177)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Deafness - small bowel diverticulosis - neuropathy (Orphanet:3217)
Dysequilibrium syndrome (Orphanet:1766)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Encephalopathy due to sulfite oxidase deficiency (Orphanet:833)
Eosinophilic granuloma (Orphanet:99871)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Familial multiple nevi flammei (Orphanet:624)
Familial or sporadic hemiplegic migraine (Orphanet:569)
Fetal iodine syndrome (Orphanet:1910)
Foodborne botulism (Orphanet:228371)
Fried syndrome (Orphanet:85335)
Fucosidosis (Orphanet:349)
Galloway-Mowat syndrome (Orphanet:2065)
Gaucher disease (Orphanet:355)
Gemignani syndrome (Orphanet:2074)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Granulomatosis with polyangiitis (Orphanet:900)
HERNS syndrome (Orphanet:63261)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Hereditary spastic paraplegia (Orphanet:685)
Hereditary vascular retinopathy (Orphanet:71291)
Hurler syndrome (Orphanet:93473)
Hydatidosis (Orphanet:400)
Hydrocephalus with stenosis of aqueduct of Sylvius (Orphanet:2182)
Hydrocephaly - tall stature - joint laxity (Orphanet:2181)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Immunoglobulin A vasculitis (Orphanet:761)
Incontinentia pigmenti (Orphanet:464)
Infantile axonal neuropathy (Orphanet:2679)
Infantile myofibromatosis (Orphanet:2591)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Infantile-onset ascending hereditary spastic paralysis (Orphanet:293168)
Intellectual deficit - microcephaly - phalangeal - facial abnormalities (Orphanet:3067)
Intellectual deficit - spasticity - ectrodactyly (Orphanet:1891)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Juvenile primary lateral sclerosis (Orphanet:247604)
KID syndrome (Orphanet:477)
Kallmann syndrome (Orphanet:478)
Kearns-Sayre syndrome (Orphanet:480)
Krabbe disease (Orphanet:487)
L1 syndrome (Orphanet:275543)
Laurence-Moon syndrome (Orphanet:2377)
Leber congenital amaurosis (Orphanet:65)
Lesch-Nyhan syndrome (Orphanet:510)
Lethal ataxia with deafness and optic atrophy (Orphanet:1187)
Locked-in syndrome (Orphanet:2406)
MASA syndrome (Orphanet:2466)
MELAS (Orphanet:550)
Macrocephaly - short stature - paraplegia (Orphanet:2427)
Maple syrup urine disease (Orphanet:511)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Monosomy 13q14 (Orphanet:1587)
Mucopolysaccharidosis type 1 (Orphanet:579)
Multiple osteochondromas (Orphanet:321)
Multiple sclerosis - ichthyosis - factor VIII deficiency (Orphanet:3151)
Muscle-eye-brain disease (Orphanet:588)
Neurocutaneous melanocytosis (Orphanet:2481)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Non-polyposis Turcot syndrome (Orphanet:99817)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculodentodigital dysplasia (Orphanet:2710)
Ophthalmoplegia - intellectual deficit - lingua scrotalis (Orphanet:2743)
PHACE syndrome (Orphanet:42775)
Palmoplantar keratoderma-spastic paralysis syndrome (Orphanet:2201)
Papilloma of choroid plexus (Orphanet:2807)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Parkes Weber syndrome (Orphanet:90307)
Peripheral hypothyroidism (Orphanet:226310)
Permanent congenital hypothyroidism (Orphanet:226292)
Perrault Syndrome (Orphanet:2855)
Pierson syndrome (Orphanet:2670)
Polyarteritis nodosa (Orphanet:767)
Porencephaly (Orphanet:2940)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Proximal spinal muscular atrophy (Orphanet:70)
Pseudoprogeria syndrome (Orphanet:2985)
Pseudoxanthoma elasticum (Orphanet:758)
Ptosis - vocal cord paralysis (Orphanet:2997)
Refsum disease (Orphanet:773)
Relapsing polychondritis (Orphanet:728)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Rett syndrome (Orphanet:778)
Rhabdoid tumor (Orphanet:69077)
Sacrococcygeal dysgenesis association (Orphanet:1773)
Scheie syndrome (Orphanet:93474)
Schizencephaly (Orphanet:799)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
Septo-optic dysplasia (Orphanet:3157)
Sinus node disease and myopia (OMIM:182190)
Sjögren-Larsson syndrome (Orphanet:816)
Sneddon syndrome (Orphanet:820)
Spastic ataxia - corneal dystrophy (Orphanet:2572)
Spastic ataxia with congenital miosis (Orphanet:1182)
Spastic diplegia, infantile type (Orphanet:1680)
Spastic paraparesis - deafness (Orphanet:2815)
Spastic paraplegia - facial-cutaneous lesions (Orphanet:2819)
Spastic paraplegia - glaucoma - intellectual deficit (Orphanet:2818)
Spastic paraplegia - nephritis - deafness (Orphanet:2820)
Spastic paraplegia - neuropathy - poikiloderma (Orphanet:2821)
Spastic paraplegia - precocious puberty (Orphanet:2826)
Spastic tetraplegia - retinitis pigmentosa - intellectual deficit (Orphanet:3011)
Spasticity - intellectual deficit - X-linked epilepsy (Orphanet:3175)
Stickler syndrome (Orphanet:828)
Tay-Sachs disease (Orphanet:845)
Thyrocerebrorenal syndrome (Orphanet:3327)
Toxin-mediated infectious botulism (Orphanet:230800)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)
Von Hippel-Lindau disease (Orphanet:892)
Worster-Drought syndrome (Orphanet:3465)
Wyburn-Mason syndrome (Orphanet:53719)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)
X-linked Charcot-Marie-Tooth disease type 2 (Orphanet:101076)
X-linked Charcot-Marie-Tooth disease type 3 (Orphanet:101077)
X-linked Charcot-Marie-Tooth disease type 5 (Orphanet:99014)
X-linked immunoneurologic disorder (Orphanet:2571)
X-linked intellectual deficit - corpus callosum agenesis - spastic quadriparesis (Orphanet:85330)
X-linked intellectual deficit, Golabi-Ito-Hall type (Orphanet:93947)