Search Ontology:
Human Disease
Joubert syndrome 16
- Term ID
- DOID:0110985
- Synonyms
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- JBTS16
- Definition
- A Joubert syndrome characterized by molar tooth sign on brain imaging, oculomotor apraxia, variable coloboma, and rare kidney involvement that has_material_basis_in homozygous mutation in the TMEM138 gene on chromosome 11q. https://www.ncbi.nlm.nih.gov/pubmed/22282472
- References
- Ontology
- Human Disease ( DOID:0110985 )
- is a type of
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Genes Involved
Zebrafish Models