DisGeNET - a database of gene-disease associations

Source: MGD

Diseases associated to the Gene: ERCC5 ×

Results per page

Gene

Disease

Variant

Source

Semantic type

Disease Class

Type

HPO Term

DO Class

CUI	Disease	Type	Disease Class	Semantic type	DO Class	HPO Term	Num. genes
C0043346	Xeroderma Pigmentosum	disease	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	Congenital Abnormality	genetic disease		9
C0268141	Xeroderma pigmentosum, group G	disease	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	Disease or Syndrome	genetic disease		1
C1968561	Xeroderma Pigmentosum, Type G-Cockayne Syndrome	disease	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases	Disease or Syndrome	genetic disease		1