Osteopathia striata cranial sclerosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Osteopathia striata with cranial sclerosis (OS-CS) is a bone dysplasia characterized by longitudinal striations of the metaphyses of the long bones, sclerosis of the craniofacial bones, macrocephaly, cleft palate and hearing loss. (Orphanet Rare Disease Ontology, Orphanet_2780)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536053
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Genes

1 genes/proteins associated with the disease Osteopathia striata cranial sclerosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
AMER1 APC membrane recruitment protein 1 2.88009