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Repository for lectin-assisted multimodality data
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MIRAGE
Bardet-Biedl syndrome 2
Summary
- Synonym
-
- BBS2
- Definition
- A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the BBS2 gene on chromosome 16q13.
- Super Class
- Bardet-Biedl syndrome
External Links
- Disease Ontology
- DOID:0110124
- Mondo Disease Ontology
- MeSH
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9BXC9 | BBSome complex member BBS2 |
