| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Wrinkly skin syndrome (WSS) is characterized by wrinkling of the skin of the dorsum of the hands and feet, an increased number of palmar and plantar creases, wrinkled abdominal skin, multiple skeletal abnormalities (joint laxity and congenital hip dislocation), late closing of the anterior fontanel, microcephaly, pre- and postnatal growth retardation, developmental delay and facial dysmorphism (a broad nasal bridge, downslanting palpebral fissures and hypertelorism). (Orphanet Rare Disease Ontology, Orphanet_2834) |
| External Link | https://www.disgenet.org/browser/0/1/0/C0406587 |
| Similar Terms | |
| Downloads & Tools |
3 genes associated with the disease Wrinkly Skin Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
