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Search the conditions that have clinical trials.
7531 conditions with clinical trials.
- Multiple congenital anomalies due to 14q32.2 imprinting defect 0 trials · 2 incl. sub-types
- Multiple intestinal atresia 0 trials · 2 incl. sub-types
- Multiple pterygium syndrome 0 trials · 2 incl. sub-types
- Necrosis of pituitary 0 trials · 2 incl. sub-types
- Neonatal osteosclerotic dysplasia 0 trials · 2 incl. sub-types
- Neuromuscular disease caused by qualitative or quantitative defects of alpha-actin 0 trials · 2 incl. sub-types
- Neuromuscular disease caused by qualitative or quantitative defects of nebulin 0 trials · 2 incl. sub-types
- Non-SCID combined immunodeficiency 0 trials · 2 incl. sub-types
- Otopalatodigital syndrome spectrum disorder 0 trials · 2 incl. sub-types
- Pallister-Hall syndrome 0 trials · 2 incl. sub-types
- Parapsoriasis 0 trials · 2 incl. sub-types
- Partial deletion of chromosome 2 0 trials · 2 incl. sub-types
- Partial deletion of the long arm of chromosome 2 0 trials · 2 incl. sub-types
- Partial deletion of the short arm of chromosome 5 0 trials · 2 incl. sub-types
- Pituitary gland infarction 0 trials · 2 incl. sub-types
- POLR3A-related disorder 0 trials · 2 incl. sub-types
- POLR3-related leukodystrophy 0 trials · 2 incl. sub-types
- POLR-related leukodystrophy 0 trials · 2 incl. sub-types
- Postsynaptic congenital myasthenic syndrome 0 trials · 2 incl. sub-types
- Qualitative or quantitative defects of delta-sarcoglycan 0 trials · 2 incl. sub-types
- Secondary hyperthyroidism 0 trials · 2 incl. sub-types
- Short rib dysplasia 0 trials · 2 incl. sub-types
- Short rib-polydactyly syndrome 0 trials · 2 incl. sub-types
- SLC26A2-related skeletal dysplasia 0 trials · 2 incl. sub-types
- SPAST-related motor disorder 0 trials · 2 incl. sub-types
- Spondylodysplastic dysplasia 0 trials · 2 incl. sub-types
- Staphylococcal toxemia 0 trials · 2 incl. sub-types
- Syndromic breast hypoplasia/aplasia 0 trials · 2 incl. sub-types
- Tricarboxylic acid cycle disorder 0 trials · 2 incl. sub-types
- Tumor grade 1 or 2, general grading system 0 trials · 2 incl. sub-types
- UROD-related inherited porphyria 0 trials · 2 incl. sub-types