OBO ID: DOID:0110996
Term Name: Joubert syndrome 27 Search Ontology:
Synonyms:
  • JBTS27
Definition: A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the B9D1 gene on chromosome 17p11. https://www.ncbi.nlm.nih.gov/pubmed/24886560
References:
Ontology: Human Disease   ( DOID:0110996 )
Relationships
is a type of:
OTHER Joubert syndrome 27 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
B9D1 Joubert syndrome 27 617120
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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