Search Ontology:
Human Disease
Bardet-Biedl syndrome 17
- Term ID
- DOID:0110139
- Synonyms
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- BBS17
- Definition
- A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the LZTFL1 gene on chromosome 3p21. (2)
- References
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- ICD10CM:Q87.89
- OMIM:615994
- Ontology
- Human Disease ( DOID:0110139 )
- is a type of
-
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