Disease #00941 (CSB (Cockayne syndrome, type B (CSB)), OMIM:133540)

Official abbreviation CSB
Name Cockayne syndrome, type B (CSB)
OMIM ID 133540
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ERCC6
Associated tissues -
Disease features -
Remarks -