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)
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Genes
6 genes involed in the disease cockayne syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
