OBO ID: DOID:0110987 |
Term Name: | Joubert syndrome 18 | Search Ontology: | |
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Synonyms: |
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Definition: | A Joubert syndrome that has_material_basis_in homozygous mutation in the TCTN3 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/22883145 | ||
References: | |||
Ontology: | Human Disease ( DOID:0110987 ) |
OTHER Joubert syndrome 18 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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TCTN3 | Joubert syndrome 18 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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