OBO ID: DOID:0110132
Term Name: Bardet-Biedl syndrome 10 Search Ontology:
Synonyms:
  • BBS10
Definition: A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the BBS10 gene on chromosome 12q21. https://www.ncbi.nlm.nih.gov/pubmed/16582908
References:
Ontology: Human Disease   ( DOID:0110132 )
Relationships
is a type of:
OTHER Bardet-Biedl syndrome 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
BBS10 Bardet-Biedl syndrome 10 615987
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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