OBO ID: DOID:0110989
Term Name: Joubert syndrome 20 Search Ontology:
Synonyms:
  • JBTS20
Definition: A Joubert syndrome that has_material_basis_in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23. https://www.ncbi.nlm.nih.gov/pubmed/23012439
References:
Ontology: Human Disease   ( DOID:0110989 )
Relationships
is a type of:
OTHER Joubert syndrome 20 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TMEM231 Joubert syndrome 20 614970
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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