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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 27/10/06 |
Symbol | CNS2 |
Location | 2q37.1 |
Name | Crigler-Najjar syndrome 2 |
Corresponding gene | UGT1A1 |
Main clinical features | mild form with reduced activity of bilirubin glucuronosyltransferase |
Genetic determination | autosomal recessive |
Function/system disorder | digestive tract/liver and annex |
Type | disease |
Remark(s) |