Occipital horn syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Occipital horn syndrome (OHS) is a mild form of Menkes disease (MD, see this term), a syndrome characterized by progressive neurodegeneration and connective tissue disorders due to a copper transport defect. (Orphanet Rare Disease Ontology, Orphanet_198)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537860
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1 genes/proteins associated with the disease Occipital horn syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ATP7A ATPase, Cu++ transporting, alpha polypeptide 2.88009