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Up to: Disorder of development or morphogenesis
Hereditary lethal multiple congenital anomalies/dysmorphic syndrome
An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.
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Meckel syndrome 0 trials · 1 incl. sub-types Sub-types →
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Bartsocas-Papas syndrome 1 0 trials
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Edinburgh malformation syndrome 0 trials
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Stromme syndrome 0 trials
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Thakker-Donnai syndrome 0 trials