OBO ID: DOID:0080278
Term Name: Joubert syndrome 32 Search Ontology:
Synonyms:
Definition: A Joubert syndrome that has_material_basis_in homozygous mutation in the SUFU gene on chromosome 10q24. https://pubmed.ncbi.nlm.nih.gov/28965847/
References:
Ontology: Human Disease   ( DOID:0080278 )
OTHER Joubert syndrome 32 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SUFU Joubert syndrome 32 617757
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None