Joubert syndrome 20

MONDO:0013994

Any Joubert syndrome in which the cause of the disease is a mutation in the TMEM231 gene.

Also known as: JBTS20, Joubert syndrome 20, Joubert syndrome caused by mutation in TMEM231, Joubert syndrome type 20, TMEM231 Joubert syndrome

36 clinical trials for this condition and its sub-types.

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