Laminopathy
MONDO:0021106A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.
25 clinical trials for this condition and its sub-types, 3 tagged with Laminopathy itself.
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Sub-types of Laminopathy
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Familial partial lipodystrophy 13 trials · 14 incl. sub-types
10 sub-types
- Familial partial lipodystrophy, Dunnigan type 4 trials
- AKT2-related familial partial lipodystrophy 0 trials
- CIDEC-related familial partial lipodystrophy 0 trials
- LIPE-related familial partial lipodystrophy 0 trials
- PLIN1-related familial partial lipodystrophy 0 trials
- PPARG-related familial partial lipodystrophy 0 trials
- Autosomal semi-dominant severe lipodystrophic laminopathy 0 trials
- Familial partial lipodystrophy, Kobberling type 0 trials
- Lipodystrophy, familial partial, type 8 0 trials
- Lipodystrophy, familial partial, type 9 0 trials
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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
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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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3 sub-types
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Atypical Werner syndrome 0 trials
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Restrictive dermopathy 1 0 trials