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Search the conditions that have clinical trials.
7595 conditions with clinical trials.
- Reactive cutaneous fibrous lesion 0 trials · 30 incl. sub-types
- Type 1 interferonopathy of childhood 0 trials · 30 incl. sub-types
- Vulvitis 0 trials · 30 incl. sub-types
- Autoinflammatory syndrome of childhood 0 trials · 29 incl. sub-types
- Autosomal dominant cerebellar ataxia type III 0 trials · 29 incl. sub-types
- Hereditary hypoparathyroidism 0 trials · 29 incl. sub-types
- Primary membranoproliferative glomerulonephritis 0 trials · 29 incl. sub-types
- Vitamin B deficiency 0 trials · 29 incl. sub-types
- Autosomal recessive metabolic cerebellar ataxia 0 trials · 28 incl. sub-types
- ELOVL4-related maculopathy 0 trials · 28 incl. sub-types
- Rhabditida infectious disease 0 trials · 28 incl. sub-types
- Urea cycle disorder or inherited hyperammonemia 0 trials · 28 incl. sub-types
- Autosomal dominant cerebellar ataxia type IV 0 trials · 27 incl. sub-types
- BEST1-related recessive retinopathy 0 trials · 27 incl. sub-types
- X-linked cone-rod dystrophy 0 trials · 27 incl. sub-types
- ATF6-related retinopathy 0 trials · 26 incl. sub-types
- Autosomal recessive limb-girdle muscular dystrophy 0 trials · 26 incl. sub-types
- CNGB1-related retinopathy 0 trials · 26 incl. sub-types
- GUCY2D-related recessive retinopathy 0 trials · 26 incl. sub-types
- GUCY2D retinopathy 0 trials · 26 incl. sub-types
- Hereditary gingival fibromatosis 0 trials · 26 incl. sub-types
- Primary optic atrophy 0 trials · 26 incl. sub-types
- RDH5-related retinopathy 0 trials · 26 incl. sub-types
- RP2-related retinopathy 0 trials · 26 incl. sub-types
- Variable-age onset idiopathic generalized epilepsy syndrome 0 trials · 26 incl. sub-types
- Autosomal recessive congenital cerebellar ataxia 0 trials · 25 incl. sub-types
- Familial nephrotic syndrome 0 trials · 25 incl. sub-types
- Familial severe combined immunodeficiency 0 trials · 25 incl. sub-types
- Neonatal-onset developmental and epileptic encephalopathy 0 trials · 25 incl. sub-types
- Abnormal mineralization disorder 0 trials · 24 incl. sub-types
- Alcohol-induced mental disorder 0 trials · 24 incl. sub-types
- Chronic non-suppurative otitis media 0 trials · 24 incl. sub-types
- Hereditary hemolytic uremic syndrome 0 trials · 24 incl. sub-types
- Inherited porphyria 0 trials · 24 incl. sub-types
- Intellectual disability, autosomal dominant 0 trials · 24 incl. sub-types
- Non-suppurative otitis media 0 trials · 24 incl. sub-types
- Opportunistic systemic mycosis 0 trials · 24 incl. sub-types
- Pyelitis 0 trials · 24 incl. sub-types
- Variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration 0 trials · 24 incl. sub-types
- Anemia, nonspherocytic hemolytic 0 trials · 23 incl. sub-types
- Digenic alpha thalassemia spectrum 0 trials · 23 incl. sub-types
- Homocystinuria without methylmalonic aciduria 0 trials · 23 incl. sub-types
- Sideroblastic anemia 0 trials · 23 incl. sub-types
- Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 0 trials · 23 incl. sub-types
- Uterine inflammatory disease 0 trials · 23 incl. sub-types
- Anemia due to erythrocyte enzyme disorder 0 trials · 22 incl. sub-types
- Congenital vitreoretinal dysplasia 0 trials · 22 incl. sub-types
- Disorder of peroxisomal transporter 0 trials · 22 incl. sub-types
- Hereditary methemoglobinemia 0 trials · 22 incl. sub-types
- Amyloidosis, hereditary systemic 1 0 trials · 21 incl. sub-types