# Diagnostic and Screening Study of Genetic Disorders

> **NCT00006057** · — · COMPLETED · sponsor: **National Center for Research Resources (NCRR)** · enrollment: 50 (—)

## Conditions studied

- Tay-Sachs Disease
- Porphyria, Erythropoietic
- Leukodystrophy, Globoid Cell
- Metabolism, Inborn Errors

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00006057
- **Lead sponsor:** National Center for Research Resources (NCRR)
- **Sponsor class:** NIH
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 1999-12
- **Primary completion:** —
- **Final completion:** —
- **Target enrollment:** 50 (—)
- **Last updated:** 2005-06-24

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00006057

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00006057, "Diagnostic and Screening Study of Genetic Disorders". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT00006057. Licensed CC0.

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