Senior-Loken syndrome

rare

Senior-Loken syndrome (SLSN) is a very rare autosomal recessive oculo-renal disease characterized by the association of nephronophthisis (NPHP), a chronic kidney disease, with retinal dystrophy.

Identifiers: MONDO:0017842 Orphanet:3156
Part of: Autosomal recessive disease Ciliopathy Inherited renal tubular disease
Also known as: nephronophthisis with retinal dystrophy · renal dysplasia retinal aplasia · renal dysplasia-retinal aplasia syndrome · Senior Loken syndrome · SLSN

Subtypes

All diseases Rare only

Disease	ID	Genes
Senior-Loken syndrome 1	MONDO:0009962	NPHP1
Senior-Loken syndrome 4	MONDO:0011756	NPHP4
Senior-Loken syndrome 5	MONDO:0012225	IQCB1
Senior-Loken syndrome 6	MONDO:0012433
Senior-Loken syndrome 7	MONDO:0013326
Senior-Loken syndrome 8	MONDO:0014579	WDR19
Senior-Loken syndrome 9	MONDO:0014712	IFT54
Nephronophthisis 15	MONDO:0013917
Senior-loken syndrome 3	MONDO:0011755

Rare disease

Projects

Including projects on subtypes.

No projects yet.