Joubert syndrome 6

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Echinobase

Summary

Literature (0)

DOID:0111001 - Joubert syndrome 6

Disease Ontology Definition:A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM67 gene on chromosome 8q22.

Synonyms: JBTS6

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tmem67

MIM:

MIM:610688 - joubert syndrome 6; jbts6

MIM:610688 - joubert syndrome 6; jbts6

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Joubert syndrome (is_a)