Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

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: April 29, 2019