OBO ID: DOID:0110139 |
Term Name: | Bardet-Biedl syndrome 17 | Search Ontology: | |
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Definition: | A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the LZTFL1 gene on chromosome 3p21. (2) | ||
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Ontology: | Human Disease ( DOID:0110139 ) |
OTHER Bardet-Biedl syndrome 17 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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