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Kufor-Rakeb Syndrome (MONDO:0011706)

Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment.

Overview

Category

nervous system disorder

Ontology ID

MONDO:0011706

Internal:12794

Synonyms

Kufor Rakeb Syndrome

Kufor-Rakeb syndrome

PARK9

KRPPD

KRS

Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia

Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia

Parkinson disease 9, autosomal recessive

Parkinson disease 9, autosomal recessive, juvenile-onset

Parkinson disease type 9

ceroid lipofuscinosis, neuronal, 12

park 9

Mapped terms

DOID:0060556

GARD:0009174

MEDGEN:338281

MESH:C537177

NORD:1959

OMIM:606693

Orphanet:306674

UMLS:C1847640

Child terms

MONDO:0017809

Results

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