CenTrial Participants with Rare Diseases
This is a live list of rare diseases that CenTrial members are seeking a clinical trial for.
If you can help any of these patients in one of your trials, please
Register with CenTrial.
If already registered please
Add a Trial to your portal.
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- Acquired adrenocortical insufficiency
- Acquired von Willebrand disease
- Acromegaly or pituitary gigantism
- Acute intermittent porphyria
- Amniotic fluid embolism
- Arthrogryposis multiplex congenita
- Autoimmune polyendocrinopathy type 2
- Bacterial endocarditis
- Benign positional paroxysmal vertigo
- Beta thalassaemia
- CADASIL - [cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome
- Central diabetes insipidus
- Cervical dystonia
- Chronic lymphocytic leukaemia or small lymphocytic lymphoma
- Cleidocranial dysplasia
- Cone rod dystrophy
- Congenital spondyloepiphyseal dysplasia
- Costochondritis
- Cystinuria
- Deficiency of cholinesterase
- Dermatitis herpetiformis
- Dermatomyositis
- Ehlers-Danlos syndrome
- Encephalitis due to herpes simplex virus
- Eosinophilic granulomatosis with polyangiitis
- Epidermolysis bullosa simplex
- Erythromelalgia
- Exstrophy of urinary bladder
- Facioscapulohumeral muscular dystrophy
- Fragile X chromosome
- Gastroschisis
- Glomerular disease with focal and segmental sclerosis
- Glycogen storage disease due to glycogen debranching enzyme deficiency
- Gorham-Stout disease
- Hemiplegic migraine
- Hereditary factor VII deficiency
- Hereditary hyperekplexia
- Hereditary thrombophilia due to congenital antithrombin deficiency
- Hyperprolactinaemia
- Hypoplastic left heart syndrome
- Idiopathic intracranial hypertension
- Immunodeficiencies with severe reduction in serum IgG or IgA with normal or elevated IgM and normal numbers of B-cells
- Incontinentia pigmenti
- Langerhans cell histiocytosis
- Lichen planus
- Long QT syndrome
- Meningiomas
- Mullerian agenesis
- Multiple endocrine neoplasia type 1
- Myasthenia gravis
- Nail-patella syndrome
- Nephrogenic diabetes insipidus
- Neurofibromatosis type 1
- Neurofibromatosis type 2
- Ocular albinism
- Osteogenesis imperfecta
- Polycythaemia vera
- Porphyria cutanea tarda
- Primary lymphoedema
- Primary tethered cord syndrome
- Pseudoxanthoma elasticum
- Pulmonary arterial hypertension
- Silver-Russell syndrome
- Spinocerebellar ataxia
- Stickler syndrome
- Stiff person syndrome
- Stress-induced cardiomyopathy
- Superior mesenteric artery syndrome of duodenum
- Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent
- Systemic sclerosis
- Tetralogy of Fallot
- Thyroid eye disease
- Transverse myelitis
- Trimethylaminuria
- Tuberous sclerosis
- Von Willebrand disease
- Von Willebrand disease type 1