Search Ontology:
Human Disease
Joubert syndrome 10
- Term ID
- DOID:0110981
- Synonyms
-
- JBTS10
- Definition
- A Joubert syndrome that has_material_basis_in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2. https://www.ncbi.nlm.nih.gov/pubmed/19800048
- References
- Ontology
- Human Disease ( DOID:0110981 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations