Hemiplegia/hemiparesis
Symptom Information:
Symptom ID: | HPO:0004374 | |||||||||||||||||||||||
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) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Paralysis and paresis (excl cranial nerve)(MedDRA:10033800) Hemiplegia/hemiparesis(HPO:0004374) |
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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) |