Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Childhood-Onset Chorea with Psychomotor Retardation (DOID:9003973)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
choreatic disease +     
3-methylglutaconic aciduria type 3  
3p deletion syndrome  
Al-Raqad Syndrome  
Alazami-Yuan Syndrome  
apraxia +   
Asparagine Synthetase Deficiency  
Bainbridge-Ropers syndrome  
Basel-Vanagaite-Smirin-Yosef syndrome  
Benign Familial Chorea  
Bowen-Conradi syndrome  
Brain-Lung-Thyroid Syndrome  
C syndrome  
cerebellar atrophy, visual impairment, and psychomotor retardation  
Childhood-Onset Chorea with Psychomotor Retardation  
chorea gravidarum 
Choreoathetosis, Familial Inverted 
Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features  
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
De Hauwere Leroy Adriaenssens syndrome 
Developmental Delay, Epilepsy, and Neonatal Diabetes  
Diaminopentanuria 
diphthamide deficiency syndrome 1  
Edinburgh Malformation Syndrome 
fumarase deficiency  
Genitopatellar Syndrome  
Glycosylphosphatidylinositol Biosynthesis Defect 15  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Harel-Yoon syndrome  
HEART AND BRAIN MALFORMATION SYNDROME  
Huntington's disease +   
Huntington's disease-like 2  
infantile cerebellar-retinal degeneration  
Infantile Hypotonia with Psychomotor Retardation +   
intellectual developmental disorder with cardiac arrhythmia  
Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN  
Keppen-Lubinsky Syndrome  
Kozlowski Rafinski Klicharska Syndrome 
MacDermot Winter Syndrome 
Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation  
Megarbane Syndrome 
mitochondrial DNA depletion syndrome 16B  
mitochondrial pyruvate carrier deficiency  
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
neuroacanthocytosis +   
Ogden syndrome  
Okur-Chung Neurodevelopmental Syndrome  
Parenti-Mignot Neurodevelopmental Syndrome  
paroxysmal nonkinesigenic dyskinesia 1  
paroxysmal nonkinesigenic dyskinesia 2 
paroxysmal nonkinesigenic dyskinesia 3  
Partial Aniridia with Unilateral Renal Agenesis and Psychomotor Retardation 
PHGDH deficiency  
polyhydramnios, megalencephaly, and symptomatic epilepsy  
PSAT deficiency  
PSPH deficiency  
Psychomotor Agitation +   
Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism  
Remitting Chorea with Nystagmus and Cataracts 
sepiapterin reductase deficiency  
THAUVIN-ROBINET-FAIVRE SYNDROME  
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Verheij Syndrome  
ZTTK syndrome  

Synonyms
Exact Synonyms: COCPMR ;   GPR88-RELATED CONDITION
Primary IDs: MIM:616939

paths to the root