
Organisations
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Ambrose Healthcare Ltd.
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Association of Medical Research Charities
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CASK Research Foundation
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CHAMP1 UK
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Congenital Conditions and Rare Diseases Registration and Information Service for Scotland (CARDRISS)
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CRELD1 Warriors
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Cure DHDDS
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Cure EB
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Cure NF2 Foundation UK & Europe
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Dravet Syndrome UK
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Early Assessment, Diagnosis and Treatment of Parkinsonism and Related Syndromes (ExPRESS) Node
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EMBL’s European Bioinformatics Institute (EMBL-EBI)
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Fahr Beyond
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Genomics England
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Hereditary Brain Aneurysm Support (HBA Support)
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HSC Research and Development Division (Northern Ireland)
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King’s Health Partners Rare Disease Network
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LifeArc
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LifeArc Centre for Rare Mitochondrial Diseases
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LifeArc Centre for Rare Respiratory Diseases
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Mary Lyon Centre
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mTOR Pathway Diseases Node
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Multiple System Atrophy Trust
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mva society
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National Disease Registration Service (NDRS)
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NHS Research Scotland
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NIHR Bioresource
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NIHR Innovation Observatory
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Northern Ireland Rare Disease Clinical and Academic Network
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Nucleic Acid Therapy Accelerator
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OpalMedica Limited
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Oxford-Harrington Rare Disease Centre
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Patient Led Research Hub
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PrimeRA Pharma Partners
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PSPA
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Rare Disease Research UK
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RD-IMAG (UK Rare Disease International Mirror and Action Group)
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RECORDER group
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SGS CDMO Solutions
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Stemnovate Limited
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The Leber’s Hereditary Optic Neuropathy Society
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The Renal Ciliopathies National Network (CILIAREN) Node
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Therapeutic Genomics CoRE
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UK Platform of Nucleic Acid Therapy for rare disease treatment (UPNAT) Node
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West Midlands Secure Data Environment