larsen syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
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)
Similar Terms
Downloads & Tools

Genes

1 genes involed in the disease larsen syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
FLNB filamin B, beta