Search Ontology:
Human Disease

Bardet-Biedl syndrome 19

Term ID
DOID:0110141
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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