Browse
Explore conditions, clinical trials, and the organisations running them.
7285 conditions with clinical trials.
- Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) 7 trials
- Autosomal dominant limb-girdle muscular dystrophy type 1F 7 trials
- Autosomal dominant limb-girdle muscular dystrophy type 1G 7 trials
- Autosomal dominant limb-girdle muscular dystrophy type 1H 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2G 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2K 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2L 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2N 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2O 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2P 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2Q 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2T 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2U 7 trials
- Autosomal recessive limb-girdle muscular dystrophy type 2X 7 trials
- Autosomal recessive polycystic kidney disease 7 trials
- Autosomal recessive primary microcephaly 7 trials
- Bardet-Biedl syndrome 7 trials
- Bilateral hypoactive labyrinth 7 trials
- Binder syndrome 7 trials
- Borderline glaucoma 7 trials
- Borrelia infectious disease 7 trials
- Breast implant illness 7 trials
- Calciphylaxis 7 trials
- Carbon monoxide poisoning 7 trials
- Central centrifugal cicatricial alopecia 7 trials
- Chalazion 7 trials
- Chandler syndrome 7 trials
- Childhood eosinophilic esophagitis 7 trials
- Chronic endometritis 7 trials
- Chronic tubotympanic suppurative otitis media 7 trials
- Cisplatin toxicity 7 trials
- Complex hereditary spastic paraplegia 7 trials
- Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency 7 trials
- Congenital disorder of glycosylation type I 7 trials
- Congenital fibrosis of extraocular muscles 7 trials
- Congenital hereditary endothelial dystrophy of cornea 7 trials
- Congenital merosin-deficient muscular dystrophy 1A 7 trials
- Congenital muscular dystrophy due to LMNA mutation 7 trials
- Congenital myasthenic syndrome 10 7 trials
- Congenital pulmonary valve stenosis 7 trials
- Creutzfeldt Jacob disease 7 trials
- Cutaneous vasculitis 7 trials
- Cyclic vomiting syndrome 7 trials
- Cystinuria 7 trials
- Demodex folliculitis 7 trials
- Demodicidosis 7 trials
- Dilated cardiomyopathy 1A 7 trials
- Disorder of GNAS inactivation 7 trials
- Disorder of iron metabolism and transport 7 trials
- Disorder of protein N-glycosylation 7 trials