Neoplasm of the liver
Symptom Information:
Symptom ID: | HPO:0002896 | ||||||||||||||||||||||||||
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) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the liver(HPO:0001392) Neoplasm of the liver(HPO:0002896) Abnormality of the gastrointestinal tract(HPO:0011024) Neoplasm of the gastrointestinal tract(HPO:0007378) Neoplasm of the liver(HPO:0002896) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Hepatobiliary neoplasms(MedDRA:10019811) Hepatobiliary neoplasms NEC(MedDRA:10019817) Neoplasm of the liver(HPO:0002896) |
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Database Frequency: | 17 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acute intermittent porphyria | (Orphanet:79276) |
Adamantinoma | (Orphanet:55881) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Beta-thalassemia intermedia | (Orphanet:231222) |
Beta-thalassemia major | (Orphanet:231214) |
Gestational trophoblastic neoplasm | (Orphanet:59305) |
Invasive mole | (Orphanet:99925) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Muir-Torre syndrome | (Orphanet:587) |
Mulibrey nanism | (Orphanet:2576) |
Nephroblastoma | (Orphanet:654) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Placental site trophoblastic tumor | (Orphanet:99928) |
Porphyria cutanea tarda | (Orphanet:101330) |
Rhabdoid tumor | (Orphanet:69077) |
Thymoma | (Orphanet:99867) |