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Solve-RD
Solving the Unsolved Rare Diseases
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The Project
WP 1: Unique RD patients and phenotypes
WP 2: Novel molecular causes
WP 3: Changing patient lives: Translation to the clinic
The Treatabolome
WP 4: Bioinformatics and knowledge management
WP 5: Engagement and impact
Community Engagement Task Force
WP 6: Coordination and innovation management
WP 7: Ethics requirements
The Group
Consortium
EKUT – 1a
EKUT – 1b
RUMC – 2
ULEIC – 3
UNEW – 4
MUH – 5
CHU Dijon – 6a
UB – 6b
CNAG-CRG – 7
EURORDIS – 8
INSERM-Orphanet – 9a
INSERM-ICM – 9b
INSERM-CRM – 9c
CUP – 10
EMBL-EBI – 11
JAX – 12
KCL – 13
UCL-IoN – 14a
UCL-ICH – 14b
UA – 15
Uni Naples – 16
UNIFE – 17
UHB – 18
IPATIMUP – 19
UMCG – 20
Charité -21
SHU – 22
APHP – 23
Project Coordinator
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Scientific Advisory Board
Independent Ethics Advisory Board
Data Analysis Task Force (DATF)
Data Interpretation Task Force (DITF)
Associated European Reference Networks
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Rare Diseases Models & Mechanisms
For Clinicians
For Model Organism Investigators
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