/Joubert syndrome 15

Joubert syndrome 15

Rare Disease

MONDO:0013763

Also Known As

CEP41 Joubert syndromeJBTS15Joubert syndrome 15Joubert syndrome caused by mutation in CEP41Joubert syndrome type 15Joubert syndrome 12/15, digenicJoubert syndrome 9/15, digenic

Definition

Any Joubert syndrome in which the cause of the disease is a mutation in the CEP41 gene.

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Associated Genes

CEP41 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614464 ↗

GARD

GARD:15806 ↗

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