Hepatocellular carcinoma
Symptom Information:
Symptom ID: | HPO:0001402 | ||||||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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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) |