OBO ID: DOID:0110141
Term Name: Bardet-Biedl syndrome 19 Search Ontology:
Synonyms:
  • BBS19
Definition: A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the IFT27 gene on chromosome 22q12. https://www.ncbi.nlm.nih.gov/pubmed/24488770
References:
Ontology: Human Disease   ( DOID:0110141 )
Relationships
is a type of:
OTHER Bardet-Biedl syndrome 19 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
IFT27 Bardet-Biedl syndrome 19 615996
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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