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Up to: Hereditary disease

Laminopathy

A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.

3 trials tagged with this condition →

Familial partial lipodystrophy 13 trials · 14 incl. sub-types Sub-types →
Hutchinson-Gilford progeria syndrome 3 trials
Adult-onset autosomal dominant demyelinating leukodystrophy 3 trials Sub-types →
Autosomal dominant Emery-Dreifuss muscular dystrophy 0 trials · 3 incl. sub-types Sub-types →
Greenberg dysplasia 2 trials
Charcot-Marie-Tooth disease type 2B1 1 trial
Buschke-Ollendorff syndrome 0 trials
Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 trials
Pelger-Huet anomaly 0 trials
X-linked Emery-Dreifuss muscular dystrophy 0 trials Sub-types →
Atypical Werner syndrome 0 trials
Mandibuloacral dysplasia with type A lipodystrophy 0 trials
Mandibuloacral dysplasia with type B lipodystrophy 0 trials
Restrictive dermopathy 1 0 trials