OBO ID: DOID:0110981
Term Name: Joubert syndrome 10 Search Ontology:
Synonyms:
  • JBTS10
Definition: A Joubert syndrome that has_material_basis_in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2. https://www.ncbi.nlm.nih.gov/pubmed/19800048
References:
Ontology: Human Disease   ( DOID:0110981 )
Relationships
is a type of:
OTHER Joubert syndrome 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
OFD1 Joubert syndrome 10 300804
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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