Search Ontology:
Human Disease
Joubert syndrome 17
- Term ID
- DOID:0110986
- Synonyms
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- JBTS17
- Definition
- A Joubert syndrome characterized by episodic hyperpnea, abnormal eye movements, ataxia, and global psychomotor retardation that has_material_basis_in compound heterozygous mutation in the C5ORF42 gene on chromosome 5p13. https://www.ncbi.nlm.nih.gov/pubmed/26092869
- References
- Ontology
- Human Disease ( DOID:0110986 )
- is a type of
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Genes Involved
Zebrafish Models