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Laminopathy
MONDO:0021106A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.
19 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Familial partial lipodystrophy
(11)
Adult-onset autosomal dominant demyelinating leukodystrophy
(2)
Emery-Dreifuss muscular dystrophy 2, autosomal dominant
(2)
Familial partial lipodystrophy, Dunnigan type
(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)