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Human Disease

Joubert syndrome 10

Term ID
DOID:0110981
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
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Other Pages
Genes Involved
Zebrafish Models