Abnormality of movement
Symptom Information:
Symptom ID: | HPO:0100022 | ||||||||||||
Synonyms: |
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Quality: | |||||||||||||
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 movement(HPO:0100022) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) |
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Database Frequency: | 129 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
14q12 microdeletion syndrome | (Orphanet:261144) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
Abetalipoproteinemia | (Orphanet:14) |
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Alpers syndrome | (Orphanet:726) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Aniridia - cerebellar ataxia - intellectual deficit | (Orphanet:1065) |
Aspartylglucosaminuria | (Orphanet:93) |
Ataxia - photosensitivity - short stature | (Orphanet:1184) |
Ataxia with vitamin E deficiency | (Orphanet:96) |
Ataxia-telangiectasia | (Orphanet:100) |
Attenuated Chédiak-Higashi syndrome | (Orphanet:352723) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant cerebellar ataxia | (Orphanet:99) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Autosomal dominant striatal neurodegeneration | (Orphanet:228169) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Benign familial chorea | (Orphanet:1429) |
Benign familial infantile seizures | (Orphanet:306) |
Cerebro-reno-digital syndrome | (Orphanet:1396) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Choreoacanthocytosis | (Orphanet:2388) |
Christianson syndrome | (Orphanet:85278) |
Chronic hiccup | (Orphanet:396) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Classic galactosemia | (Orphanet:79239) |
Cockayne syndrome | (Orphanet:191) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital intrauterine infection-like syndrome | (Orphanet:1229) |
Corneal-cerebellar syndrome | (Orphanet:3177) |
De Barsy syndrome | (Orphanet:2962) |
Diencephalic syndrome | (Orphanet:1672) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Dopa-responsive dystonia | (Orphanet:255) |
Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
Dysequilibrium syndrome | (Orphanet:1766) |
Early-onset generalized limb-onset dystonia | (Orphanet:256) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Encephalopathy due to sulfite oxidase deficiency | (Orphanet:833) |
Erythrokeratodermia - ataxia | (Orphanet:1955) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Flynn-Aird syndrome | (Orphanet:2047) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
GM1 gangliosidosis | (Orphanet:354) |
Galactosemia | (Orphanet:352) |
Gaucher disease | (Orphanet:355) |
German syndrome | (Orphanet:2077) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Griscelli disease | (Orphanet:381) |
Griscelli disease type 1 | (Orphanet:79476) |
HERNS syndrome | (Orphanet:63261) |
Hepatic fibrosis - renal cysts - intellectual deficit | (Orphanet:2031) |
Hereditary continuous muscle fiber activity | (Orphanet:972) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary hyperekplexia | (Orphanet:3197) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Huntington disease | (Orphanet:399) |
Infant botulism | (Orphanet:178478) |
Infantile axonal neuropathy | (Orphanet:2679) |
Infantile convulsions and choreoathetosis | (Orphanet:31709) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Intellectual deficit, X-linked - plagiocephaly | (Orphanet:2898) |
Intellectual deficit, X-linked - psychosis - macroorchidism | (Orphanet:3077) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |
Isolated cerebellar hypoplasia/agenesis | (Orphanet:1398) |
Kallmann syndrome | (Orphanet:478) |
Kennedy disease | (Orphanet:481) |
Leber hereditary optic neuropathy | (Orphanet:104) |
Leigh syndrome | (Orphanet:506) |
Lesch-Nyhan syndrome | (Orphanet:510) |
MERRF | (Orphanet:551) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Methylmalonic acidemia with homocystinuria | (Orphanet:26) |
Methylmalonic acidemia with homocystinuria, type cblD | (Orphanet:79283) |
Microlissencephaly - micromelia | (Orphanet:50810) |
Monomelic amyotrophy | (Orphanet:65684) |
Muscle-eye-brain disease | (Orphanet:588) |
Myoclonus - cerebellar ataxia - deafness | (Orphanet:2589) |
Nasu-Hakola disease | (Orphanet:2770) |
Neonatal adrenoleukodystrophy | (Orphanet:44) |
Neuhauser-Eichner-Opitz syndrome | (Orphanet:2672) |
Neuroectodermal melanolysosomal disease | (Orphanet:33445) |
Neuroferritinopathy | (Orphanet:157846) |
Neuronal ceroid lipofuscinosis | (Orphanet:216) |
Neuronal intranuclear inclusion disease | (Orphanet:2289) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Oxoglutaricaciduria | (Orphanet:31) |
PEHO syndrome | (Orphanet:2836) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Pelizaeus-Merzbacher disease | (Orphanet:702) |
Pellagra-like skin rash-neurological manifestations | (Orphanet:2837) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Perrault Syndrome 5 | (OMIM:616138) |
Perry syndrome | (Orphanet:178509) |
Pierson syndrome | (Orphanet:2670) |
Porencephaly | (Orphanet:2940) |
Primary orthostatic tremor | (Orphanet:238606) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Psychogenic movement disorders | (Orphanet:71519) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Rett syndrome | (Orphanet:778) |
Roussy-Lévy syndrome | (Orphanet:3115) |
Sandhoff disease | (Orphanet:796) |
Sialidosis type 1 | (Orphanet:812) |
Sialidosis type 2 | (Orphanet:87876) |
Spasmus nutans | (Orphanet:279882) |
Spastic paraparesis - deafness | (Orphanet:2815) |
Tay-Sachs disease | (Orphanet:845) |
Tremor - nystagmus - duodenal ulcer | (Orphanet:3350) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Williams syndrome | (Orphanet:904) |
Wilson disease | (Orphanet:905) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome | (Orphanet:85295) |
X-linked sideroblastic anemia - ataxia | (Orphanet:2802) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |