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Explore conditions, clinical trials, and the organisations running them.
7285 conditions with clinical trials.
- Disorder of fatty acid and ketone body metabolism 18 trials
- Disseminated intravascular coagulation 18 trials
- Dystonia, focal, task-specific 18 trials
- Early-onset generalized dystonia 18 trials
- Factor VII deficiency 18 trials
- Generalized dystonia 18 trials
- GM2 gangliosidosis 18 trials
- Hemoglobin H disease 18 trials
- Hereditary anemia 18 trials
- Hereditary hyperbilirubinemia 18 trials
- Hypogonadism, male 18 trials
- Idiopathic recurrent pericarditis 18 trials
- Immunoproliferative disorder 18 trials
- Joubert syndrome and related disorders 18 trials
- Kennedy disease 18 trials
- Lafora disease 18 trials
- Lymphadenitis 18 trials
- Machado-Joseph disease type 3 18 trials
- Mesial temporal lobe epilepsy with hippocampal sclerosis 18 trials
- Methylmalonic aciduria and homocystinuria 18 trials
- Moderately severe hemophilia A 18 trials
- Mucopolysaccharidosis type 1 18 trials
- Neuronitis 18 trials
- Nominal aphasia 18 trials
- Osteochondritis dissecans 18 trials
- Partial deletion of chromosome 7 18 trials
- Partial deletion of the long arm of chromosome 7 18 trials
- Partial lipodystrophy 18 trials
- Persian gulf syndrome 18 trials
- Postgastrectomy syndrome 18 trials
- Progressive muscular atrophy 18 trials
- Proliferative vitreoretinopathy 18 trials
- Red-green color blindness 18 trials
- Retinoschisis 18 trials
- Sandhoff disease 18 trials
- Spinocerebellar ataxia 9 18 trials
- Spinocerebellar ataxia type 23 18 trials
- Spinocerebellar ataxia type 27 18 trials
- Spinocerebellar ataxia type 29 18 trials
- Sterile multifocal osteomyelitis with periostitis and pustulosis 18 trials
- Toxic or drug-related embryofetopathy 18 trials
- Transient familial neonatal hyperbilirubinemia 18 trials
- TREX1-related type 1 interferonopathy 18 trials
- Unverricht-Lundborg syndrome 18 trials
- Uterine inflammatory disease 18 trials
- Williams syndrome 18 trials
- Yellow fever 18 trials
- Young-onset Parkinson disease 18 trials
- Abdominal wall malformation 17 trials
- Acid sphingomyelinase deficiency 17 trials