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| Term | Bardet-Biedl syndrome 21 | ID (Ontology) | DOID:0081010 (Human Disease) |
| Definition | A Bardet-Biedl syndrome that is characterized by obesity, postaxial polydactyly, retinal degeneration, and mild cognitive impairment and that has_material_basis_in homozygous mutation in the C8ORF37 gene on chromosome 8q22. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal recessive disease__ syndrome_____________________| Bardet-Biedl syndrome |__Bardet-Biedl syndrome 21 |
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| Is a | Bardet-Biedl syndrome | ||
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| MIM:617406 | |||