Mondo Disease Ontology
2766 terms(s) returned
| Term Type: | Record: 1351 to 1400 of 2766 Records | Page: 28 of 56, First Previous Next Last | Show Records Per Page |
- hepatitis, viral, animal
- hepatobiliary benign neoplasm
- hepatobiliary disorder
- hepatobiliary neoplasm
- hepatobiliary system
- hepatoblast
- hepatoblastoma
- hepatoblastoma, non-human animal
- hepatocellular adenoma
- hepatocellular carcinoma
- hepatocellular carcinoma in situ, non-human animal
- hepatocellular carcinoma, non-human animal
- hepatocellular clear cell carcinoma
- hepatocellular fibrinogen storage disease, DGKG-related, cattle
- hepatocellular fibrinogen storage disease, non-human animal
- hepatocutaneous syndrome, non-human animal
- hepatocyte
- hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
- hepatoerythropoietic porphyria
- hepatogenous photosensitization, non-human animal
- hepatoid adenocarcinoma
- hepatomegaly, non-human animal
- hepatopancreatic ampulla
- hepatopathy, non-human animal
- hepatoportal sclerosis
- hepatoprotective agent
- hepatopulmonary syndrome
- hepatorenal syndrome
- hepatorenocardiac degenerative fibrosis
- hepatosplenic T-cell lymphoma
- hepatotoxic agent
- hepatotoxicity, non-human animal
- herbicide
- hereditary North American Indian childhood cirrhosis
- hereditary Wilms tumor
- hereditary acrokeratotic poikiloderma, Weary type
- hereditary alpha tryptasemia syndrome
- hereditary amyloidosis
- hereditary anemia
- hereditary angioedema
- hereditary angioedema type 1
- hereditary angioedema type 2
- hereditary angioedema type 3
- hereditary angioedema with C1Inh deficiency
- hereditary angioedema with normal C1Inh
- hereditary angioedema with normal C1inh not related to F12 or PLG variant
- hereditary anorectal anomalies
- hereditary antithrombin deficiency
- hereditary arterial and articular multiple calcification syndrome
- hereditary ataxia
