PomBase home

Disease association ontology term - MONDO:0021095 - parkinsonian disorder

Term summary

ID
MONDO:0021095
Name
parkinsonian disorder
Ontology or CV name
Disease association
Definition
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.

Parents

Annotation

Disease association

MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23

References:

Genes:

MONDO:0011658 - autosomal recessive early-onset Parkinson disease 7

References:

Genes:

MONDO:0014233 - early-onset Parkinson disease 20

References:

Genes:

MONDO:0011706 - Kufor-Rakeb syndrome

References:

Genes:

MONDO:0008199 - late-onset Parkinson disease

References:

Genes:

MONDO:0005180 - Parkinson disease

References:

Genes:

MONDO:0013625 - Parkinson disease 17

References:

Genes:

MONDO:0014742 - Parkinson disease 22, autosomal dominant

References:

Genes:

MONDO:0957576 - Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development

References:

Genes:

MONDO:0030676 - parkinsonism-dystonia 3, childhood-onset

References:

Genes:

MONDO:0008201 - Perry syndrome

References:

Genes:

MONDO:0010747 - X-linked dystonia-parkinsonism

References:

Genes: