OBO ID: DOID:0110135
Term Name: Bardet-Biedl syndrome 13 Search Ontology:
Synonyms:
  • BBS13
Definition: A Bardet-Biedl syndrome that has_material_basis_in compound heterozygous mutation in the MKS1 gene on chromosome 17q22. https://www.ncbi.nlm.nih.gov/pubmed/18327255
References:
Ontology: Human Disease   ( DOID:0110135 )
Relationships
is a type of:
OTHER Bardet-Biedl syndrome 13 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MKS1 Bardet-Biedl syndrome 13 615990
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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