About: Congenital mirror movement disorder

Facets (new session)
Description
Metadata
Settings
- Rule:
- Inverse Functional Properties:
- "Same As":

About: Congenital mirror movement disorder Goto Sponge NotDistinct Permalink

An Entity of Type : dbo:Disease, within Data Space : dbpedia.org associated with source document(s)
QRcode icon

http://dbpedia.org/describe/?url=http%3A%2F%2Fdbpedia.org%2Fresource%2FCongenital_mirror_movement_disorder

Congenital mirror movement disorder (CMM disorder) is a rare genetic neurological disorder which is characterized by mirrored movement, sometimes referred to as associated or synkinetic movement, most often in the upper extremity of the body. These movements are voluntary intentional movements on one, ipsilateral, side of the body that are mirrored simultaneously by involuntary movements on the contralateral side.

Attributes	Values
rdf:type	Thing Disease disease
rdfs:label	Congenital mirror movement disorder (en) اضطراب حركة المرآة (ar) Mouvements en miroir familiaux congénitaux (fr)
rdfs:comment	Les mouvements en miroir familiaux congénitaux ou mouvements en miroir congénitaux sont une maladie génétique neurologique qui se caractérise par l'apparition précoce de mouvements involontaires reproduisant selon un axe de symétrie droite-gauche les mouvements effectués du côté opposé de façon volontaire. (fr) اضطراب حركة المرآة (congenital mirror movement disorder)، مرض جيني عصبي نادر، غالباً ما يكون في أطراف الجسد العلوية، عند الحركة الإرادية في جانبٍ واحد من الجسد يقوم الجانب الأخر بذات الحركة في الوقت نفسه لا إرادياً. (ar) Congenital mirror movement disorder (CMM disorder) is a rare genetic neurological disorder which is characterized by mirrored movement, sometimes referred to as associated or synkinetic movement, most often in the upper extremity of the body. These movements are voluntary intentional movements on one, ipsilateral, side of the body that are mirrored simultaneously by involuntary movements on the contralateral side. (en)
foaf:name	Congenital mirror movement disorder (en)
name	Congenital mirror movement disorder (en)
foaf:depiction
dcterms:subject	Extrapyramidal and movement disorders
Wikipage page ID	34489456 (xsd:integer)
Wikipage revision ID	1100056480 (xsd:integer)
Link from a Wikipage to another Wikipage	Extrapyramidal and movement disorders Profession Schizophrenia Epilepsy Mutation Nervous system Primary motor cortex Alien hand syndrome Appendage DCC1 DNA Developmental biology Dynein Infant Insertion (genetics) Penetrance Corpus callosum Medullary pyramids (brainstem) Gene expression Genetic disorder Genetic testing Genome Genome-wide association study Genotype Nonsense mutation Midline shift Rare disease Zygosity RAD51 Gene Movement disorders Corticospinal tract Clinical trial Commissural fiber Pain Social stigma Stop codon Symmetry in biology Symptom Cerebral hemisphere Cerebral palsy DNAL4 Amino acid Amyotrophic lateral sclerosis Anatomical terms of location Anatomy Dystonia Parkinson's disease Cell migration Frameshift mutation Motor cortex Obsessive–compulsive disorder Protein Receptor (biochemistry) Accelerometer Acquired brain injury Chiari malformation Kallmann syndrome Kangaroo Heredity Homologous recombination Workforce Dexterity Dominance (genetics) Axon Axon guidance Phenotype Intellectual disability Klippel–Feil syndrome Meckel syndrome Netrin 1 Neurological disorder Exome sequencing Exon Manual labour Wildervanck syndrome Myelin Möbius syndrome Molecular biology Motor neuron Splice site mutation Skeletal muscle Cognitive disability Interhemispheric fissure Subclinical

Faceted Search & Find service v1.17_git139 as of Feb 29 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 08.03.3330 as of Mar 19 2024, on Linux (x86_64-generic-linux-glibc212), Single-Server Edition (62 GB total memory, 42 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software