Search Ontology:
Human Disease
Joubert syndrome 34
- Term ID
- DOID:0061336
- Synonyms
-
- JBTS34
- Definition
- A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the B9D2 gene on chromosome 19q13.2. https://pubmed.ncbi.nlm.nih.gov/26092869/
- References
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- MIM:614175
- ORDO:564
- Ontology
- Human Disease ( DOID:0061336 )
Other Pages
Genes Involved
Zebrafish Models