Search Ontology:
Human Disease
Bardet-Biedl syndrome 2
- Term ID
- DOID:0110124
- Synonyms
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- BBS2
- 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
- References
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- GARD:821
- ICD10CM:Q87.89
- MESH:C537910
- MIM:615981
- Ontology
- Human Disease ( DOID:0110124 )
- is a type of
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Genes Involved
Zebrafish Models