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Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary disease
Laminopathy
A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.
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Familial partial lipodystrophy 13 trials · 14 incl. sub-types Sub-types →
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Hutchinson-Gilford progeria syndrome 3 trials
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Autosomal dominant Emery-Dreifuss muscular dystrophy 0 trials · 3 incl. sub-types Sub-types →
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Greenberg dysplasia 2 trials
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Buschke-Ollendorff syndrome 0 trials
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Pelger-Huet anomaly 0 trials
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Atypical Werner syndrome 0 trials
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Restrictive dermopathy 1 0 trials