Search Ontology:
Human Disease
Bardet-Biedl syndrome 13
- Term ID
- DOID:0110135
- Synonyms
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- BBS13
- Definition
- A Bardet-Biedl syndrome that has_material_basis_in compound heterozygous mutation in the MKS1 gene on chromosome 17q22. https://www.ncbi.nlm.nih.gov/pubmed/18327255
- References
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- ICD10CM:Q87.89
- MESH:C567140
- MIM:615990
- Ontology
- Human Disease ( DOID:0110135 )
- is a type of
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Genes Involved
Zebrafish Models