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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

0 clinical trials for this condition and its sub-types, 0 tagged with Joubert syndrome 10 itself.

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Part of

↑ Joubert syndrome (2) ↑ OFD1-related ciliopathy (1)

Including sub-types (0) Tagged with Joubert syndrome 10 (0)

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