| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An X-linked disease characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern. (Human Disease Ontology, DOID_14711) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537923 |
| Similar Terms | |
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5 genes/proteins associated with the disease Opitz-Kaveggia syndrome from the curated CTD Gene-Disease Associations dataset.
