Search Ontology:
Human Disease

Bardet-Biedl syndrome 17

Term ID
DOID:0110139
Synonyms
  • 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
Ontology
Human Disease   ( DOID:0110139 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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