Abnormality of the liver

Symptom Information:

Symptom ID: HPO:0001392
Synonyms:
Liver abnormality [HPO:0001392]
Liver disease [HPO:0001392]
Liver disease [OMIM:Liver disease]
Liver disease (in some patients) [OMIM:Liver disease (in some patients)]
Quality:
Cross references:
OMIM: "Liver disease" [OMIM:Liver disease]
OMIM: "Liver disease (in some patients)" [OMIM:Liver disease (in some patients)]
Is a (Direct Parents):
HPO         Decreased carnitine level in liver
HPO         Abnormality of the abdominal organs
HPO         Abnormal liver parenchyma morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
MedDRA:
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 13 (OMIM:615990)
Bardet-Biedl syndrome 6 (OMIM:605231)
Blue rubber bleb nevus (Orphanet:1059)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
Congenital atransferrinemia (Orphanet:1195)
Fetal Gaucher disease (Orphanet:85212)
GM1 gangliosidosis type 2 (Orphanet:79256)
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO (OMIM:240150)
Hepatic veno-occlusive disease - immunodeficiency (Orphanet:79124)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
Mediterranean macrothrombocytopenia (Orphanet:101022)
Menkes disease (Orphanet:565)
Microcytic anemia with liver iron overload (Orphanet:83642)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Nephronophthisis 2 (OMIM:602088)
Nephronophthisis 3 (OMIM:604387)
Nephronophthisis 9 (OMIM:613824)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 (OMIM:610131)
Retroperitoneal fibrosis (Orphanet:49041)
Tyrosinemia type 3 (Orphanet:69723)
Von Hippel-Lindau disease (Orphanet:892)
Wilson disease (Orphanet:905)