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disease > genetic disease > hereditary disease > Joubert syndrome
... > disease > nervous system diseases > neurological disorder > psychomotor disorder > psychomotor retardation > Joubert syndrome
disease > respiratory disease > Joubert syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > ataxia > cerebellar ataxia > Joubert syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > Joubert syndrome
... > disease > striated muscle disease > dystonia > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > Joubert syndrome
... > disease > nervous system diseases > neurological disorder > involuntary movement > dystonia > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > Joubert syndrome
... > disease > nervous system diseases > neurological disorder > involuntary movement > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > Joubert syndrome
... > disease > nervous system diseases > neurological disorder > involuntary movement > dyskinesia > ataxia > cerebellar ataxia > Joubert syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > cerebellar disease > cerebellar ataxia > Joubert syndrome
disease > eye disease > oculomotor syndrome > abnormal eye movement > Joubert syndrome

Preferred term

Joubert syndrome  

Definition

  • Joubert syndrome is a rare autosomal recessive genetic disorder that affects the cerebellum, an area of the brain that controls balance and coordination. (Wikipedia)

Broader concept

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URI

http://data.loterre.fr/ark:/67375/VH8-ZZD1C200-G

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