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Disease association ontology term - MONDO:0017755 - inborn disorder of bilirubin metabolism

Term summary

ID
MONDO:0017755
Name
inborn disorder of bilirubin metabolism
Ontology or CV name
Disease association
Definition
An instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome.

Parents

Annotation

Disease association

MONDO:0008822 - arthrogryposis, renal dysfunction, and cholestasis 1

References:

Genes:

MONDO:0017123 - arthrogryposis-renal dysfunction-cholestasis syndrome

References:

Genes:

MONDO:0011559 - benign recurrent intrahepatic cholestasis type 2

References:

Genes:

MONDO:0030810 - cholestasis, progressive familial intrahepatic, 10

References:

Genes:

MONDO:0031040 - cholestasis, progressive familial intrahepatic, 12

References:

Genes:

MONDO:0009380 - Dubin-Johnson syndrome

References:

Genes:

MONDO:0011156 - progressive familial intrahepatic cholestasis type 2

References:

Genes:

MONDO:0011214 - progressive familial intrahepatic cholestasis type 3

References:

Genes: