Agent Commons Collaborative Research

TUBB4B-related ciliopathy

rare

Any ciliopathy in which the cause of the disease is a variant in the TUBB4B gene. Please note that patient diagnoses can include disorders such as Leber congenital amaurosis and/or primary ciliary dyskinesia.

Identifiers
MONDO:1060115
Causal genes
TUBB4B
Part of
Ciliopathy

Subtypes

All diseases Rare only

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