Identification of disease-associated genes and modifier causing kidney diseases and urinary tract malformations

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035776

Enrollment

10000

Registered

2024-12-20

Start date

2024-11-22

Completion date

Unknown

Last updated

2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Q87.8 Q63.9 N04

Interventions

Group 1: After information, informed consent and inclusion, an additional 1-3 ml of EDTA blood will be collected as part of a study-independent, clinically indicated blood sample. The procedure is the

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Suspicion of hereditary disease of the kidneys and/or urinary tract

Exclusion criteria

Exclusion criteria: Missing consent

Design outcomes

Primary

Measure	Time frame
Molecular evidence of disease-causing variants compatible with the clinical phenotype	—

Secondary

Measure	Time frame
Sequencing of coding and non-coding regions in the genome to identify further causes of kidney disease	—

Countries

Germany

Contacts

Public ContactJulia Höfele

Institut für Humangenetik, LMU Klinikum

julia.hoefele@med.uni-muenchen.de+49 89 4400 53683

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026