Hepatocellular carcinoma

Symptom Information:

Symptom ID: HPO:0001402
Synonyms:
Increased hepatocellular carcinoma risk [HPO:0001402]
Increased incidence of hepatocellular carcinoma [HPO:0001402]
Hepatocellular carcinoma [OMIM:Hepatocellular carcinoma]
Increased hepatocellular carcinoma risk [OMIM:Increased hepatocellular carcinoma risk]
Increased incidence of hepatocellular carcinoma [OMIM:Increased incidence of hepatocellular carcinoma]
Hepatocellular carcinoma [MedDRA:10073071]
Quality:
Cross references:
OMIM: "Hepatocellular carcinoma" [OMIM:Hepatocellular carcinoma]
OMIM: "Increased hepatocellular carcinoma risk" [OMIM:Increased hepatocellular carcinoma risk]
OMIM: "Increased incidence of hepatocellular carcinoma" [OMIM:Increased incidence of hepatocellular carcinoma]
Is a (Direct Parents):
MedDRA Malignant hepatobiliary neoplasms
HPO         Neoplasm of the liver
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the gastrointestinal tract(HPO:0007378)
                Neoplasm of the liver(HPO:0002896)
                   Hepatocellular carcinoma(HPO:0001402)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Neoplasm of the gastrointestinal tract(HPO:0007378)
                   Neoplasm of the liver(HPO:0002896)
                      Hepatocellular carcinoma(HPO:0001402)
             Abnormality of the liver(HPO:0001392)
                Neoplasm of the liver(HPO:0002896)
                   Hepatocellular carcinoma(HPO:0001402)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Hepatobiliary neoplasms(MedDRA:10019811)
       Malignant hepatobiliary neoplasms(MedDRA:10025577)
          Hepatocellular carcinoma(HPO:0001402)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

Acute intermittent porphyria (Orphanet:79276)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Alpha-1-antitrypsin deficiency (Orphanet:60)
Argininemia (Orphanet:90)
Budd-Chiari syndrome (Orphanet:131)
Citrullinemia type II (Orphanet:247585)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Hemochromatosis, type 1 (OMIM:235200)
Hepatocellular carcinoma (Orphanet:88673)
Hepatoerythropoietic porphyria (Orphanet:95159)
Navajo neurohepatopathy (Orphanet:255229)
Progressive familial intrahepatic cholestasis type 2 (Orphanet:79304)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
RUIJS-AALFS SYNDROME (OMIM:616200)
SILVER-RUSSELL SYNDROME (OMIM:180860)
Silver-Russell syndrome (Orphanet:813)
Tyrosinemia type 1 (Orphanet:882)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)