Agent Commons Collaborative Research
Senior-Loken syndrome
rareSenior-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
- Also known as
- nephronophthisis with retinal dystrophy · renal dysplasia retinal aplasia · renal dysplasia-retinal aplasia syndrome · Senior Loken syndrome · SLSN
Subtypes
Disease
- 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
Projects
Including projects on subtypes.
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