PomBase home

Disease association ontology term - MONDO:0005154 - liver disorder

Term summary

ID
MONDO:0005154
Name
liver disorder
Ontology or CV name
Disease association
Definition
A disease involving the liver.

Parents

Annotation

Disease association

MONDO:0013111 - acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

References:

Genes:

MONDO:0008294 - acute intermittent porphyria

References:

Genes:

MONDO:0000447 - autosomal dominant polycystic liver disease

References:

Genes:

MONDO:0011559 - benign recurrent intrahepatic cholestasis type 2

References:

Genes:

MONDO:0013995 - cholestasis, intrahepatic, of pregnancy, 3

References:

Genes:

MONDO:0030810 - cholestasis, progressive familial intrahepatic, 10

References:

Genes:

MONDO:0031040 - cholestasis, progressive familial intrahepatic, 12

References:

Genes:

MONDO:0958224 - encephalopathy, porphyria-related

References:

Genes:

MONDO:0001676 - erythropoietic protoporphyria

References:

Genes:

MONDO:0008296 - familial porphyria cutanea tarda

References:

Genes:

MONDO:0002520 - hepatic porphyria

References:

Genes:

MONDO:0007256 - hepatocellular carcinoma

References:

Genes:

MONDO:0007369 - hereditary coproporphyria

References:

Genes:

MONDO:0024568 - infantile liver failure syndrome 1

References:

Genes:

MONDO:0014659 - infantile liver failure syndrome 2

References:

Genes:

MONDO:0032844 - infantile liver failure syndrome 3

References:

Genes:

MONDO:0958226 - leukoencephalopathy, porphyria-related

References:

Genes:

MONDO:0024477 - liver and intrahepatic bile duct neoplasm

References:

Genes:

MONDO:0008265 - polycystic liver disease 1

References:

Genes:

MONDO:0014860 - polycystic liver disease 2

References:

Genes:

MONDO:0054743 - polycystic liver disease 3 with or without kidney cysts

References:

Genes:

MONDO:0015104 - porphyria cutanea tarda

References:

Genes:

MONDO:0013000 - porphyria due to ALA dehydratase deficiency

References:

Genes:

MONDO:0011156 - progressive familial intrahepatic cholestasis type 2

References:

Genes:

MONDO:0011214 - progressive familial intrahepatic cholestasis type 3

References:

Genes:

MONDO:0008319 - protoporphyria, erythropoietic, 1

References:

Genes:

MONDO:0013771 - transient infantile hypertriglyceridemia and hepatosteatosis

References:

Genes:

MONDO:0008297 - variegate porphyria

References:

Genes:

MONDO:0957577 - variegate porphyria, childhood-onset

References:

Genes:

MONDO:0010420 - X-linked erythropoietic protoporphyria

References:

Genes: