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Joubert syndrome 10

MONDO:0010431

Any Joubert syndrome in which the cause of the disease is a mutation in the OFD1 gene.

Also known as: JBTS10, Joubert syndrome 10, Joubert syndrome 10, X-linked recessive, Joubert syndrome caused by mutation in OFD1, Joubert syndrome type 10, OFD1 Joubert syndrome

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

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Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) 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)
Trials to join now! 1 Completed 1
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