| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB, see this term) and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes. (Orphanet Rare Disease Ontology, Orphanet_2908) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C536321 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Poikiloderma of Kindler from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| FERMT1 | fermitin family member 1 | 2.88009 |
