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Disease association ontology term - MONDO:0011706 - Kufor-Rakeb syndrome

Term summary

ID
MONDO:0011706
Name
Kufor-Rakeb syndrome
Ontology or CV name
Disease association
Definition
Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment.

Parents

Annotation

Disease association

MONDO:0011706 - Kufor-Rakeb syndrome

References:

Genes: