Rigid spine syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Rigid spine syndrome (RSS) is a slowly progressive childhood-onset congenital muscular dystrophy (see this term) characterized by contractures of the spinal extensor muscles associated with abnormal posture (limitation of neck and trunk flexure), progressive scoliosis of the spine, early marked cervico-axial muscle weakness with relatively preserved strength and function of the extremities and progressive respiratory insufficiency. (Orphanet Rare Disease Ontology, Orphanet_97244)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535683
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Rigid spine syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SEPN1 selenoprotein N, 1 2.88009