Disease Browser
Parent Node: Dyskinesias (D020820) Parent Node: Psychomotor Disorders (D011596) ..Starting node .. Psychomotor Agitation (D011595) Child Nodes:
........Akathisia, Drug-Induced (D017109) Sister Nodes: ..Apraxias (D001072) 10 ..Bowen-Conradi syndrome (C537081) ..C SYNDROME (OMIM:211750) ..CHROMOSOME 3pter-p25 DELETION SYNDROME (OMIM:613792) ..De Hauwere Leroy Adriaenssens syndrome (C535991) ..Developmental Delay, Epilepsy, and Neonatal Diabetes (C565253) ..Diaminopentanuria (C565630) ..Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency (C562657) ..Edinburgh Malformation Syndrome (C563051) ..Fumaric aciduria (C538191) ..Genitopatellar Syndrome (C565255) ..Growth Retardation, Small and Puffy Hands and Feet, and Eczema (C565528) ..Hypomyelination, Global Cerebral (C567847) ..Ichthyosis prematurity syndrome (C536271) ..Kozlowski Rafinski Klicharska syndrome (C537509) ..MacDermot Winter syndrome (C537714) ..Megarbane syndrome (C536145) ..Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay (C563345) ..Phosphoglycerate Dehydrogenase Deficiency (C566618) ..Phosphoserine Aminotransferase Deficiency (C567032) ..Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy (C567020) ..Psychomotor Agitation (D011595) 1 ..Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 9447
Name: Psychomotor Agitation
Definition: A feeling of restlessness associated with increased motor activity. This may occur as a manifestation of nervous system drug toxicity or other conditions.
Alternative IDs:
ParentIDs: MESH:D011596|MESH:D020820
TreeNumbers: C10.597.350.600 |C10.597.606.881.700 |C23.888.592.350.600 |C23.888.592.604.882.700
Synonyms: Agitation, Psychomotor |Akathisia |Excitement, Psychomotor |Hyperactivity, Psychomotor |Psychomotor Excitement |Psychomotor Hyperactivity |Psychomotor Restlessness |Restlessness |Restlessness, Psychomotor
Slim Mappings: Nervous system disease|Signs and symptoms
Reference:
MedGen: D011595
MeSH: D011595
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants