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Explore conditions, clinical trials, and the organisations running them.
7285 conditions with clinical trials.
- Nezelof syndrome 2 trials
- Non-SCID combined immunodeficiency 2 trials
- Norum disease 2 trials
- Nose, anomalous shape of 2 trials
- Null syndrome 2 trials
- Ocular albinism 2 trials
- Ocular toxoplasmosis 2 trials
- Odonto-onycho-dermal dysplasia 2 trials
- Orchitis 2 trials
- Orofacial cleft 1 2 trials
- Otopalatodigital syndrome spectrum disorder 2 trials
- Pallister-Hall syndrome 2 trials
- Paralytic lagophthalmos 2 trials
- Paronychia 2 trials
- Partial deletion of chromosome 2 2 trials
- Partial deletion of the long arm of chromosome 2 2 trials
- Partial deletion of the short arm of chromosome 5 2 trials
- Partial duplication of the long arm of chromosome 15 2 trials
- Parturient paresis 2 trials
- Pelizaeus-Merzbacher-like disease 2 trials
- Peptic ulcer perforation 2 trials
- Periodic paralysis 2 trials
- Pfeiffer syndrome 2 trials
- Phimosis 2 trials
- Physiological malfunction arising from mental factor 2 trials
- Pili bifurcati 2 trials
- Pituitary apoplexy 2 trials
- Pituitary gland infarction 2 trials
- Pituitary hormone deficiency, combined, 1 2 trials
- Plastic bronchitis 2 trials
- Platelet aggregation, spontaneous 2 trials
- Poland syndrome 2 trials
- POLR3A-related disorder 2 trials
- POLR3-related leukodystrophy 2 trials
- POLR-related leukodystrophy 2 trials
- Polycystic kidney disease 1 2 trials
- Polydactyly-myopia syndrome 2 trials
- Polyhydramnios 2 trials
- Polymorphic light eruption 2 trials
- Popliteal cyst 2 trials
- Portal vein, cavernous transformation of 2 trials
- Portosinusoidal vascular disease 2 trials
- Postaxial acrofacial dysostosis 2 trials
- Postprandial hypotension 2 trials
- Postsynaptic congenital myasthenic syndrome 2 trials
- Potter sequence 2 trials
- Pregnancy associated osteoporosis 2 trials
- Primary hyperoxaluria type 3 2 trials
- Primary progressive apraxia of speech 2 trials
- Proximal symphalangism 2 trials