Search Ontology:
Human Disease

Joubert syndrome 32

Term ID
DOID:0080278
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models