Search Ontology:
Human Disease
Joubert syndrome 3
- Term ID
- DOID:0110998
- Synonyms
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- 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 )
- is a type of
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