Myoclonus
Symptom Information:
Symptom ID: | HPO:0001336 | |||||||||||||||||||||||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Involuntary movements(HPO:0004305) Myoclonus(HPO:0001336) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Involuntary movements(HPO:0004305) Myoclonus(HPO:0001336) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Neurological signs and symptoms NEC(MedDRA:10029306) Myoclonus(HPO:0001336) |
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Database Frequency: | 115 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALZHEIMER DISEASE 3 | (OMIM:607822) |
ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA | (OMIM:208700) |
ATAXIA-TELANGIECTASIA | (OMIM:208900) |
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Alpers syndrome | (Orphanet:726) |
Alpha-N-acetylgalactosaminidase deficiency | (Orphanet:3137) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Alpha-N-acetylgalactosaminidase deficiency type 3 | (Orphanet:79281) |
Alström syndrome | (Orphanet:64) |
Amish infantile epilepsy syndrome | (Orphanet:171714) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Ataxia-telangiectasia | (Orphanet:100) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal recessive ataxia due to ubiquinone deficiency | (Orphanet:139485) |
Autosomal recessive cerebellar ataxia - saccadic intrusion | (Orphanet:95434) |
Autosomal recessive dopa-responsive dystonia | (Orphanet:101150) |
Autosomal recessive dopa-responsive dystonia | (Orphanet:101150) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
CEREBELLOPARENCHYMAL DISORDER V | (OMIM:213400) |
CLN1 disease | (Orphanet:228329) |
CLN2 disease | (Orphanet:228349) |
CLN3 disease | (Orphanet:228346) |
CLN4A disease | (Orphanet:228340) |
CLN4B disease | (Orphanet:228343) |
CLN5 disease | (Orphanet:228360) |
CLN8 disease | (Orphanet:228354) |
CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET | (OMIM:217200) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Creutzfeldt-Jakob disease | (Orphanet:204) |
D-glyceric aciduria | (Orphanet:941) |
DYSTONIA 15, MYOCLONIC | (OMIM:607488) |
DYSTONIA 23 | (OMIM:614860) |
Dentatorubral pallidoluysian atrophy | (Orphanet:101) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY | (OMIM:615924) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 | (OMIM:607876) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3 | (OMIM:613608) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7 | (OMIM:604827) |
EPILEPSY, MYOCLONIC JUVENILE | (OMIM:254770) |
EPILEPSY, PROGRESSIVE MYOCLONIC 7 | (OMIM:616187) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
Early-onset spastic ataxia-neuropathy syndrome | (Orphanet:313772) |
Encephalopathy due to GLUT1 deficiency | (Orphanet:71277) |
Encephalopathy due to prosaposin deficiency | (Orphanet:139406) |
Familial cortical myoclonus | (Orphanet:319189) |
Familial encephalopathy with neuroserpin inclusion bodies | (Orphanet:85110) |
Fatal familial insomnia | (Orphanet:466) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Glycine encephalopathy | (Orphanet:407) |
Guanidinoacetate methyltransferase deficiency | (Orphanet:382) |
HYPEREKPLEXIA, HEREDITARY 1 | (OMIM:149400) |
Hereditary hyperekplexia | (Orphanet:3197) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
Lafora disease | (Orphanet:501) |
Late infantile neuronal ceroid lipofuscinosis | (Orphanet:168491) |
Leber plus disease | (Orphanet:99718) |
Leigh syndrome | (Orphanet:506) |
Leprechaunism | (Orphanet:508) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 | (OMIM:616158) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6 | (OMIM:611092) |
MERRF | (Orphanet:551) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Myoclonus - cerebellar ataxia - deafness | (Orphanet:2589) |
Myoclonus-dystonia syndrome | (Orphanet:36899) |
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED | (OMIM:256700) |
NYSTAGMUS, MYOCLONIC | (OMIM:310800) |
Nasu-Hakola disease | (Orphanet:2770) |
Navajo neurohepatopathy | (Orphanet:255229) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neonatal hemochromatosis | (Orphanet:446) |
Neuroblastoma | (Orphanet:635) |
Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency | (Orphanet:88639) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
PARASOMNIA, SLEEP BRUXISM TYPE | (OMIM:606840) |
POLYMYOCLONUS, INFANTILE | (OMIM:263550) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Pontocerebellar hypoplasia type 4 | (Orphanet:166063) |
Primary dystonia, DYT6 type | (Orphanet:98806) |
Progressive myoclonic epilepsy type 6 | (Orphanet:280620) |
Progressive myoclonic epilepsy with dystonia | (Orphanet:352596) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Pyridoxal phosphate-responsive seizures | (Orphanet:79096) |
Pyruvate carboxylase deficiency | (Orphanet:3008) |
RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1 | (OMIM:102300) |
RFT1-CDG | (Orphanet:244310) |
Ramsay-Hunt syndrome | (Orphanet:3020) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |
Sialidosis type 1 | (Orphanet:812) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 19/22 | (Orphanet:98772) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
Thyrocerebrorenal syndrome | (Orphanet:3327) |
Unverricht-Lundborg disease | (Orphanet:308) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked dystonia-parkinsonism | (Orphanet:53351) |
X-linked intellectual disability due to GRIA3 anomalies | (Orphanet:364028) |
Young adult-onset Parkinsonism | (Orphanet:2828) |