Abnormality of movement

Symptom Information:

Symptom ID: HPO:0100022
Synonyms:
Movement disorder [HPO:0100022]
Movement disorder [Orphanet:43220]
Movement disorder (disorder) [Orphanet:43220]
Movement Disorders [Orphanet:43220]
Movement disorder [OMIM:Movement disorder]
Movement disorder [MedDRA:10028035]
Movement disorder NOS [MedDRA:10028035]
Movements disturbance NOS [MedDRA:10028035]
Movement disorder (NOS) [MedDRA:10028035]
Decreased arm swing [MedDRA:10028035]
Movement disorders [OMIM:Movement disorders]
Movement disorders (incl parkinsonism) [MedDRA:10028037]
Quality:
Cross references:
Orphanet:43220 "Movement disorder" [Orphanet:43220]
OMIM: "Movement disorder" [OMIM:Movement disorder]
OMIM: "Movement disorders" [OMIM:Movement disorders]
UMLS:C0026650 "Movement Disorders" [Orphanet:43220]
Is a (Direct Parents):
Orphanet [DEL]Motor deficit/trouble
MedDRA Dyskinesias and movement disorders NEC
MedDRA Nervous system disorders
HPO         Abnormality of nervous system physiology
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)
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)