Cure My Disease

Don't miss your cure!

Log in / Sign up

Laminopathy

MONDO:0021106

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

21 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Familial partial lipodystrophy (11) Adult-onset autosomal dominant demyelinating leukodystrophy (3) Familial partial lipodystrophy, Dunnigan type (3) Emery-Dreifuss muscular dystrophy 2, autosomal dominant (2) Greenberg dysplasia (2) Hutchinson-Gilford progeria syndrome (2) AKT2-related familial partial lipodystrophy (0) Atypical Werner syndrome (0) Autosomal dominant Emery-Dreifuss muscular dystrophy (0) Autosomal semi-dominant severe lipodystrophic laminopathy (0) Buschke-Ollendorff syndrome (0) Charcot-Marie-Tooth disease type 2B1 (0) CIDEC-related familial partial lipodystrophy (0) Emery-Dreifuss muscular dystrophy 1, X-linked (0) Emery-Dreifuss muscular dystrophy 3, autosomal recessive (0) Emery-Dreifuss muscular dystrophy 4, autosomal dominant (0) Emery-Dreifuss muscular dystrophy 5, autosomal dominant (0) Emery-Dreifuss muscular dystrophy 6, X-linked (0) Emery-Dreifuss muscular dystrophy 7, autosomal dominant (0) Familial partial lipodystrophy, Kobberling type (0)

Broader categories

Disease (680) Hereditary disease (176) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0)

Trials to join now! 11 Not yet finished but already full! 4 Completed 4 Terminated 2