Dubin-Johnson syndrome
(Q1263039)
rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum
rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum
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Current Data About
Dubin-Johnson syndrome
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q390475)
(Q55785261)
(Q12136) |
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| (P1748) |
C34741
C34741
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| (P1995) |
(Q123028)
(Q668064) |
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| (P2293) |
(Q17907816)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_12308
http://identifiers.org/doid/DOID:12308
http://www.orpha.net/ORDO/Orphanet_234 |
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| (P5008) |
(Q4099686)
|
other details
| aliases |
Dubin Johnson syndrome chronic idiopathic jaundice Hyperbilirubinemia 2 DJS Sprinz-Nelson syndrome Hyperbilirubinemia, Dubin-Johnson Type Hyperbilirubinemia type 2 DUBIN-JOHNSON SYNDROME; DJS Dubin-Sprinz disease DUBIN-JOHNSON SYNDROME |
| description | rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum |
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