Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Joubert syndrome 18
Summary
- Synonym
-
- JBTS18
- Definition
- A Joubert syndrome that has_material_basis_in homozygous mutation in the TCTN3 gene on chromosome 10q24.
- Super Class
- Joubert syndrome
External Links
- Disease Ontology
- DOID:0110987
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001251 | Ataxia |
| HP:0002876 | Episodic tachypnea |
| HP:0000508 | Ptosis |
| HP:0002084 | Encephalocele |
| HP:0000369 | Low-set ears |
| HP:0001320 | Cerebellar vermis hypoplasia |
| HP:0002269 | Abnormality of neuronal migration |
| HP:0000864 | Abnormality of the hypothalamus-pituitary axis |
| HP:0000238 | Hydrocephalus |
| HP:0001696 | Situs inversus totalis |
