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Laminopathy

MONDO:0021106

A 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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Where it sits in the disease tree

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Part of

↑ Hereditary disease (18187)

Sub-types of Laminopathy

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
Hutchinson-Gilford progeria syndrome 3 trials
Adult-onset autosomal dominant demyelinating leukodystrophy 3 trials
2 sub-types
- Leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypical 0 trials
- Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical 0 trials
Autosomal dominant Emery-Dreifuss muscular dystrophy 0 trials · 3 incl. sub-types
4 sub-types
- Emery-Dreifuss muscular dystrophy 2, autosomal dominant 3 trials
- Emery-Dreifuss muscular dystrophy 4, autosomal dominant 0 trials
- Emery-Dreifuss muscular dystrophy 5, autosomal dominant 0 trials
- Emery-Dreifuss muscular dystrophy 7, autosomal dominant 0 trials
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
3 sub-types
- Emery-Dreifuss muscular dystrophy 1, X-linked 0 trials
- Emery-Dreifuss muscular dystrophy 6, X-linked 0 trials
- X-linked myopathy with postural muscle atrophy 0 trials
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

Including sub-types (25) Tagged with Laminopathy (3)

Trials to join now! 12 Not yet recruiting 2 Not yet finished but already full! 4 Completed 5 Terminated 2

Laminopathy

Where it sits in the disease tree

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