Joubert Syndrome 14
Disease ID: disease_node_14703
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| Dbxref | MIM:614424 |
|---|---|
| Subclassof | DOID_0050777 |
| Data Source | DOID |
| Synonyms | JBTS14 |
| Doid Label | Joubert syndrome 14 |
| Doid Description | A Joubert syndrome characterized by severe mental retardation, hypoplasia of the cerebellar vermis and molar tooth sign on brain imaging, hypotonia, abnormal breathing pattern in infancy, and dysmorphic facial features that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM237 gene on chromosome 2q33. |
| Disease Node Id | disease_node_14703 |
| Doid Id | DOID_0110983 |
| Label | Joubert Syndrome 14 |
- Outgoing r'ship
SUBCLASS_OFto/from Joubert Syndrome(ID:disease_node_14692) (Disease)