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Human Disease

Cockayne syndrome A

Term ID
DOID:0080907
Synonyms
  • Cockayne syndrome type 1
  • Cockayne syndrome type I
Definition
A Cockayne syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the group 8 excision repair cross-complementing protein on chromosome 5q11. https://medlineplus.gov/genetics/condition/cockayne-syndrome/
References
Ontology
Human Disease   ( DOID:0080907 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models