Search Ontology:
Human Disease
Bardet-Biedl syndrome 16
- Term ID
- DOID:0110138
- Synonyms
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- BBS16
- Definition
- A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the SDCCAG8 gene on chromosome 1q43. (2)
- References
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- ICD10CM:Q87.89
- OMIM:615993
- Ontology
- Human Disease ( DOID:0110138 )
- is a type of
-
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