OBO ID: DOID:0110124
Term Name: Bardet-Biedl syndrome 2 Search Ontology:
Synonyms:
  • BBS2
Definition: A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the BBS2 gene on chromosome 16q13. https://www.ncbi.nlm.nih.gov/pubmed/16823392
References:
Ontology: Human Disease   ( DOID:0110124 )
OTHER Bardet-Biedl syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
BBS2 Bardet-Biedl syndrome 2 615981
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None