DISEASES

Disease-gene associations mined from literature

Human genes for dyskeratosis congenita

Dyskeratosis congenita [DOID:2729]

A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity.

Synonyms:  dyskeratosis congenita,  DOID:2729

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8