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| Term | Joubert syndrome | ID (Ontology) | DOID:0050777 (Human Disease) |
| Definition | A ciliopathy that is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones. | ||
| Also Known As | "JBTS" | ||
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| Is a |
ciliopathy brain disease |
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GARD:6802 ICD10CM:Q04.3 MIM:PS213300 ORDO:475 |
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