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Human Disease

Joubert syndrome 17

Term ID
DOID:0110986
Synonyms
  • 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 )
Relationships
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Genes Involved
Zebrafish Models