Search Ontology:
Human Disease
Joubert syndrome 15
- Term ID
- DOID:0110984
- Synonyms
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- JBTS15
- Definition
- A Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has_material_basis_in homozygous mutation in the CEP41 gene on chromosome 7q32. https://www.ncbi.nlm.nih.gov/pubmed/22246503
- References
- Ontology
- Human Disease ( DOID:0110984 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models