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Explore conditions, clinical trials, and the organisations running them.
7477 conditions with clinical trials.
- Frontometaphyseal dysplasia 2 trials
- Frontometaphyseal dysplasia 2 2 trials
- Fucosidosis 2 trials
- Galactosialidosis 2 trials
- Gas bloat syndrome 2 trials
- Gastrin secretion abnormality 2 trials
- Gastrointestinal anthrax 2 trials
- Gastrointestinal defect and immunodeficiency syndrome 2 trials
- Gastrointestinal defects and immunodeficiency syndrome 1 2 trials
- Generalized dominant dystrophic epidermolysis bullosa 2 trials
- Generalized resistance to thyroid hormone 2 trials
- General tumor grading characteristic 2 trials
- Glyceronephosphate O-acyltransferase deficiency 2 trials
- Glycogen storage disease due to GLUT2 deficiency 2 trials
- Glycogen storage disease due to glycogen branching enzyme deficiency 2 trials
- Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency 2 trials
- Glycogen storage disease due to muscle and heart glycogen synthase deficiency 2 trials
- Glycogen storage disease III 2 trials
- Glycogen storage disease VI 2 trials
- Glycogen storage disorder due to hepatic glycogen synthase deficiency 2 trials
- Granuloma annulare 2 trials
- Granuloma inguinale 2 trials
- Grouped pigmentation of the retina 2 trials
- GYG1-related disorder of glycogen metabolism 2 trials
- HELIX syndrome 2 trials
- Hemimelia 2 trials
- Hepatitis, infectious canine 2 trials
- Hepatitis, non-human animal 2 trials
- Hepatitis, viral, animal 2 trials
- Histoplasma capsulatum infectious disease 2 trials
- Holocarboxylase synthetase deficiency 2 trials
- Hyaline fibromatosis syndrome 2 trials
- Hyalohyphomycosis 2 trials
- Hypercholesterolemia, autosomal dominant, type B 2 trials
- Hyperkalemic periodic paralysis 2 trials
- Hypermature cataract 2 trials
- Hypertrophic lichen planus 2 trials
- Hypoalphalipoproteinemia, primary, 1 2 trials
- Hypomyelinating leukodystrophy 5 2 trials
- Hypomyelinating leukodystrophy 6 2 trials
- Hypomyelination with brain stem and spinal cord involvement and leg spasticity 2 trials
- Hypophosphatemic rickets, autosomal recessive, 2 2 trials
- Hypothyroidism, congenital, nongoitrous 2 trials
- Hypothyroidism due to TSH receptor mutations 2 trials
- Hypotrichosis of eyelid 2 trials
- Hypouricemia, renal 1 2 trials
- Idiopathic mast cell activation syndrome 2 trials
- Immature cataract 2 trials
- Immunodeficiency due to selective anti-polysaccharide antibody deficiency 2 trials
- Inherited cutis laxa 2 trials