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| Term | Joubert syndrome 24 | ID (Ontology) | DOID:0110993 (Human Disease) |
| Definition | A Joubert syndrome characterized by delayed psychomotor development and molar tooth sign on brain MRI that has_material_basis_in homozygous mutation in the TCTN2 gene on chromosome 12q24. | ||
| Also Known As | "JBTS24" | ||
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ciliopathy_____ brain disease__| Joubert syndrome |__Joubert syndrome 24 |
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| Is a | Joubert syndrome | ||
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| MIM:616654 | |||