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Metadata
ID	DOID:0110981
Name	Joubert syndrome 10
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
Xrefs	MESH:C567582 MIM:300804
Synonyms	JBTS10 [EXACT]
Parent Relationships	is_a Joubert syndrome is_a X-linked recessive disease
Subclass Logical Relationships	has material basis in some X-linked recessive inheritance