ATELOSTEOGENESIS, TYPE III Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=OMIM:108721
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Genes

1 genes/proteins associated with the disease ATELOSTEOGENESIS, TYPE III from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FLNB filamin B, beta 2.88009