atelosteogenesis, type iii Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atelosteogenesis III (AOIII) is a skeletal dysplasia characterized by short limbs dysmorphic facies and diagnostic radiographic findings. (Orphanet Rare Disease Ontology, Orphanet_56305)
External Link http://www.omim.org/entry/108721
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Genes

1 genes associated with the atelosteogenesis, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FLNB filamin B, beta