General Information of Disease (ID: DISFPEQA)

Disease Name Laminopathy
Definition A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.
Disease Hierarchy
DISYKSRF: Genetic disease
DISWD40R: Disease
DISFPEQA: Laminopathy
Disease Identifiers
MONDO ID
MONDO_0021106
MESH ID
D000083083
UMLS CUI
C5392094
MedGen ID
1716073
Orphanet ID
98301