Joubert syndrome 11

Joubert syndrome 11 is an autosomal dominant and recessive disorder caused by mutations of the TTC21B gene.

Systematic

Joubert syndrome
	Joubert syndrome 01
	Joubert syndrome 02
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	Joubert syndrome 06
	Joubert syndrome 07
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	Joubert syndrome 09
	Joubert syndrome 10
	Joubert syndrome 11
		TTC21B
	Joubert syndrome 12
	Joubert syndrome 13
	Joubert syndrome 14
	Joubert syndrome 15
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	Joubert syndrome 17
	Joubert syndrome 18
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	Joubert syndrome 21
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	Joubert syndrome 35

References:

1.	Davis EE et al. (2011) TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.

2.	OMIM.ORG article Omim 613820

Update: June 23, 2025

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