Ontology Browser

Parent Terms Term With Siblings Child Terms
movement disease +     
Akathisia, Drug-Induced 
Alopecia, Hypogonadism, Extrapyramidal Disorder 
Angelman syndrome  
basal ganglia calcification +   
basal ganglia cerebrovascular disease +  
benign shuddering attacks 
Beta-Ureidopropionase Deficiency  
biotin-responsive basal ganglia disease  
chorea gravidarum 
choreatic disease +   
congenital mirror movement disorder +   
Dyskinesias +   
dystonia +   
Dystonia Musculorum Deformans +   
Early Onset Parkinsonism with Mental Retardation  
extrapyramidal and movement disease 
frontotemporal dementia +   
Gilles de la Tourette syndrome +   
guanidinoacetate methyltransferase deficiency  
Huntington's disease +   
Meige syndrome 
multiple system atrophy +   
Neuhauser Eichner Opitz Syndrome 
neuroleptic malignant syndrome 
Non-Lissencephalic Cortical Dysplasia 
Pallidal Degeneration, Progressive, with Retinitis Pigmentosa 
pantothenate kinase-associated neurodegeneration +   
Parkinsonian Disorders +   
A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.
progressive supranuclear palsy +   
Pronation-Supination Of The Forearm, Impairment Of 
Spastic Paraplegia with Associated Extrapyramidal Signs 
Stiff-Person syndrome  
syndromic X-linked intellectual disability 5  
Telfer Sugar Jaeger Syndrome 
tic disorder +   
Wilson disease +   
Woodhouse Sakati Syndrome  

Exact Synonyms: Autosomal Dominant Juvenile Parkinsonism ;   Autosomal Dominant Parkinsonism ;   Autosomal Recessive Juvenile Parkinson Disease ;   Autosomal Recessive Parkinsonism ;   Autosomal Recesssive Juvenile Parkinsonism ;   Chromosome 6 Linked Autosomal Recessive Parkinsonism ;   ECTOL1 ;   EPDF ;   Experimental Parkinson Disease ;   Experimental Parkinson Diseases ;   Experimental Parkinsonism ;   Experimental Parkinsonisms ;   Familial Juvenile Parkinsonism ;   Familial Parkinson Disease, Autosomal Recessive ;   Juvenile Parkinson Disease ;   Juvenile Parkinsonism ;   Juvenile Parkinsonism, Autosomal Recessive ;   Juvenile Parkinsonisms ;   MPTP Induced Experimental Parkinsonism ;   PDJ ;   Parkinsonian Diseases ;   Parkinsonian Disorders ;   Parkinsonian Syndrome ;   Parkinsonian Syndromes ;   Parkinsonism ;   Ramsay Hunt paralysis syndrome ;   autosomal dominant juvenile Parkinson disease
Primary IDs: MESH:D020734
Alternate IDs: RDO:0002965

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.