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Diseases

Gilbert Disease (Disorder)

gilbert disease (disorder)

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Gilbert Disease (Disorder)
Standard Disease Name
gilbert disease (disorder)
MeSH Tree
No data
ICD-10
E80.4

Identifiers

DO ID
No data
MeSH ID
D005878
OMIM ID
191740|143500|MTHU031877
UMLS ID
C0017551
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.|MSH2017_2016_08_12:A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
CYP2D6
cytochrome P450 family 2 subfamily D member 6
cytochrome P450 family 2 subfamily D member 6
08
UGT1A5
UDP glucuronosyltransferase family 1 member A5
UDP glucuronosyltransferase family 1 member A5