OBO ID: DOID:0111004
Term Name: Joubert syndrome 9 Search Ontology:
Synonyms:
  • JBTS9
Definition: A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15. https://www.ncbi.nlm.nih.gov/pubmed/18387594
References:
Ontology: Human Disease   ( DOID:0111004 )
Relationships
is a type of:
OTHER Joubert syndrome 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CC2D2A Joubert syndrome 9 612285
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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