Nephronophthisis 19

Nephronophthisis type 19 is an autosomal recessive disorder caused by mutations in the DCDC2 gene.

Systematic

Nephronophthisis
	Nephronophthisis 01
	Nephronophthisis 02
	Nephronophthisis 03
	Nephronophthisis 04
	Nephronophthisis 05
	Nephronophthisis 06
	Nephronophthisis 07
	Nephronophthisis 08
	Nephronophthisis 09
	Nephronophthisis 10
	Nephronophthisis 11
	Nephronophthisis 12
	Nephronophthisis 13
	Nephronophthisis 14
	Nephronophthisis 15
	Nephronophthisis 16
	Nephronophthisis 17
	Nephronophthisis 18
	Nephronophthisis 19
		DCDC2
	Nephronophthisis 20
	Nephronophthisis-like nephropathy 1

References:

1.	Schueler M et al. (2015) DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling.

2.	OMIM.ORG article Omim 616217

Update: June 23, 2025

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