# Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings

> **NCT04315727** · NA · UNKNOWN · sponsor: **University Hospital Tuebingen** · enrollment: 100 (estimated)

## Conditions studied

- Rare Diseases
- Genetic Predisposition to Disease

## Interventions

- **GENETIC:** WGS Diagnostic Blood take for genetic diagnostic.
- **GENETIC:** Hair collection

## Key facts

- **NCT ID:** NCT04315727
- **Lead sponsor:** University Hospital Tuebingen
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2021-02-01
- **Primary completion:** 2024-07
- **Final completion:** 2024-12
- **Target enrollment:** 100 (ESTIMATED)
- **Last updated:** 2023-11-29


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04315727

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04315727, "Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT04315727. Licensed CC0.

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