Search Ontology:
Human Disease
Bardet-Biedl syndrome 22
- Term ID
- DOID:0081011
- Synonyms
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- Definition
- A Bardet-Biedl syndrome that is retinitis pigmentosa, obesity, polydactyly, hypogonadism, and intellectual disability has_material_basis_in compound heterozygous or homozygous mutation in the IFT74 gene on chromosome 9p21. https://pubmed.ncbi.nlm.nih.gov/27486776/
- References
- Ontology
- Human Disease ( DOID:0081011 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models