OBO ID: DOID:0110998
Term Name: Joubert syndrome 3 Search Ontology:
Synonyms:
  • JBTS3
Definition: A Joubert syndrome that has_material_basis_in homozygous mutation in the AHI1 gene on chromosome 6q23.3. https://www.ncbi.nlm.nih.gov/pubmed/15322546
References:
Ontology: Human Disease   ( DOID:0110998 )
Relationships
is a type of:
OTHER Joubert syndrome 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AHI1 Joubert syndrome 3 608629
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.