CTRI/2021/12/038519尚未招募未知
Center for Rare Disease Diagnosis, Research and Training
DBT Wellcome Trust India Alliance0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Individuals of any age and of both genders with a possible genetic disorder can be a part of the study
排除标准
- •Individuals with acquired conditions or multifactorial diseases
研究者
相似试验
已完成
不适用
Central Information Portal for rare diseases - Sub-project 2: Information Request from patients and their families.Rare diseases.DRKS00006011niversität Hannover - Center for Health Economics Research92
Unknown
不适用
Rare and Undiagnosed Disease Research BiorepositoryUndiagnosed DiseaseRare DiseasesNCT04703179Mayo Clinic5,000
招募中
不适用
Precision Diagnosis and Therapy for Rare Diseases by Interpreting Non-coding GenomesGenetic DiseaseNCT06775561IRCCS Azienda Ospedaliero-Universitaria di Bologna100
Unknown
不适用
Functional Tests to Resolve Unsolved Rare Diseases. Rares.Rubinstein-Taybi SyndromeCongenital Heart DefectPeriventricular Nodular HeterotopiaNeurodegeneration With Brain Iron Accumulation (NBIA)Cystic FibrosisAlbinismIntellectual DisabilityNCT05696912University Hospital, Bordeaux50
招募中
不适用
Diagnostic Research in Patients With Rare Diseases - Solving the Unsolved Rare DiseasesRare DiseasesGenetic PredispositionNCT03491280University Hospital Tuebingen5,500