OBO ID: DOID:0110987
Term Name: Joubert syndrome 18 Search Ontology:
Synonyms:
  • JBTS18
Definition: A Joubert syndrome that has_material_basis_in homozygous mutation in the TCTN3 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/22883145
References:
Ontology: Human Disease   ( DOID:0110987 )
OTHER Joubert syndrome 18 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TCTN3 Joubert syndrome 18
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None