Larsen Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities. (Human Disease Ontology, DOID_14764)
External Link https://www.disgenet.org/browser/0/1/0/C1837884
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Genes

6 genes associated with the disease Larsen Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL7A1 collagen, type VII, alpha 1
FLNB filamin B, beta
GZF1 GDNF-inducible zinc finger protein 1
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)