Atelosteogenesis type 1 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Atelosteogenesis I is a perinatally lethal skeletal dysplasia characterized by severe short-limbed dwarfism, joint dislocations, club feet along with distinctive facies and radiographic findings. (Orphanet Rare Disease Ontology, Orphanet_1190)
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1 genes associated with the Atelosteogenesis type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
FLNB filamin B, beta