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Joubert syndrome 24

MONDO:0014724

Any Joubert syndrome in which the cause of the disease is a mutation in the TCTN2 gene.

Also known as: JBTS24, Joubert syndrome 24, Joubert syndrome caused by mutation in TCTN2, Joubert syndrome type 24, TCTN2 Joubert syndrome

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

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Broader categories

Disease (680) Hereditary disease (176) Syndromic disease (25) Human disease (14) Ciliopathy (2) Disease by molecular mechanism (2) Disease of genetic or genomic mechanism (2) Joubert syndrome (2) Disease by body system or component (0) Disease by developmental or physiological process (0)

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