laminopathy
MONDO:0021106Mondo
Findings
No curated finding names laminopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.
Definition from the Mondo Disease Ontology (MONDO:0021106), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (14)
- adult-onset autosomal dominant demyelinating leukodystrophy
- atypical Werner syndrome
- autosomal dominant Emery-Dreifuss muscular dystrophy
- Buschke-Ollendorff syndrome
- Charcot-Marie-Tooth disease type 2B1
- Emery-Dreifuss muscular dystrophy 3, autosomal recessive
- familial partial lipodystrophy
- Greenberg dysplasia
- Hutchinson-Gilford progeria syndrome
- mandibuloacral dysplasia with type A lipodystrophy
- mandibuloacral dysplasia with type B lipodystrophy
- Pelger-Huet anomaly
- restrictive dermopathy 1
- X-linked Emery-Dreifuss muscular dystrophy