| Disease Browser
|
Parent Node:
 Neurobehavioral Manifestations (D019954) | ..Starting node
.. Psychomotor Disorders (D011596)
|
Child 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) |
Sister Nodes: | ..Anhedonia (D059445)
| ..Apraxias (D001072) 10
| ..Catatonia (D002389) 1
| ..Communication Disorders (D003147) 57
| ..Confusion (D003221) 2
| ..Consciousness Disorders (D003244) 11
| ..Intellectual Disability (D008607) 579
| ..Lethargy (D053609)
| ..Memory Disorders (D008569) 7
| ..Perceptual Disorders (D010468) 13
| ..Psychomotor Disorders (D011596) 34
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
|
|
|
| Term ID: | 9448 |
| Name: | Psychomotor Disorders |
| Definition: | Abnormalities of motor function that are associated with organic and non-organic cognitive disorders. |
| Alternative IDs: | |
| ParentIDs: | MESH:D019954 |
| TreeNumbers: | C10.597.606.881 |C23.888.592.604.882 |
| Synonyms: | Developmental Psychomotor Disorder |Developmental Psychomotor Disorders |Impairment, Psychomotor |Impairments, Psychomotor |Psychomotor Disorder, Developmental |Psychomotor Disorders, Developmental |Psychomotor Impairment |Psychomotor Impairments |
| Slim Mappings: | Nervous system disease|Signs and symptoms |
| Reference: |
MedGen: D011596
MeSH: D011596
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
|
