OBO ID: DOID:0110124 |
Term Name: | Bardet-Biedl syndrome 2 | Search Ontology: | |
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Definition: | A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the BBS2 gene on chromosome 16q13. https://www.ncbi.nlm.nih.gov/pubmed/16823392 | ||
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Ontology: | Human Disease ( DOID:0110124 ) |
OTHER Bardet-Biedl syndrome 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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