Disease association ontology term - MONDO:0024431 - bilirubin metabolism disease
Term summary
ID
MONDO:0024431
Name
bilirubin metabolism disease
Ontology or CV name
Disease association
Parents
is_a
metabolic disease
Annotation
Disease association
MONDO:0008822
-
arthrogryposis, renal dysfunction, and cholestasis 1
References:
PB_REF:0000006
Genes:
vps33 (SPBC1703.15c)
MONDO:0017123
-
arthrogryposis-renal dysfunction-cholestasis syndrome
References:
PB_REF:0000003
Genes:
vps33 (SPBC1703.15c)
MONDO:0011559
-
benign recurrent intrahepatic cholestasis type 2
References:
PB_REF:0000006
Genes:
pmd1 (SPCC663.03)
MONDO:0030810
-
cholestasis, progressive familial intrahepatic, 10
References:
PB_REF:0000006
Genes:
myo51 (SPBC2D10.14c)
myo52 (SPCC1919.10c)
MONDO:0031040
-
cholestasis, progressive familial intrahepatic, 12
References:
PB_REF:0000006
Genes:
vps33 (SPBC1703.15c)
MONDO:0009380
-
Dubin-Johnson syndrome
References:
PB_REF:0000006
Genes:
abc1 (SPAC9E9.12c)
abc2 (SPAC3F10.11c)
abc3 (SPBC359.05)
abc4 (SPAC30.04c)
MONDO:0011156
-
progressive familial intrahepatic cholestasis type 2
References:
PB_REF:0000006
Genes:
pmd1 (SPCC663.03)
MONDO:0011214
-
progressive familial intrahepatic cholestasis type 3
References:
PB_REF:0000006
Genes:
pmd1 (SPCC663.03)
