| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An autosomal recessive disease that is caused by rare mutations in two DNA excision repair proteins, ERCC-8 and ERCC-6, and characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. (Human Disease Ontology, DOID_2962) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D003057 |
| Similar Terms | |
| Downloads & Tools |
2 genes/proteins associated with the disease Cockayne Syndrome from the curated CTD Gene-Disease Associations dataset.
