gracile bone dysplasia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Osteocraniostenosis is a lethal skeletal dysplasia characterized by a cloverleaf skull anomaly, facial dysmorphism, limb shortness, splenic hypo/aplasia and radiological anomalies including thin tubular bones with flared metaphyses and deficient calvarial mineralization. (Orphanet Rare Disease Ontology, Orphanet_2763)
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1 genes associated with the gracile bone dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FAM111A family with sequence similarity 111, member A