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| Term | Bardet-Biedl syndrome 2 | ID (Ontology) | DOID:0110124 (Human Disease) |
| Definition | A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the BBS2 gene on chromosome 16q13. | ||
| Also Known As | "BBS2" | ||
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autosomal recessive disease__ syndrome_____________________| Bardet-Biedl syndrome |__Bardet-Biedl syndrome 2 |
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| Is a | Bardet-Biedl syndrome | ||
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GARD:821 ICD10CM:Q87.89 MESH:C537910 MIM:615981 |
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