Mondo Disease Ontology
2494 terms(s) returned
| Term Type: | Record: 1201 to 1250 of 2494 Records | Page: 25 of 50, First Previous Next Last | Show Records Per Page |
- hepatitis C virus, susceptibility to
- hepatitis D virus infection
- hepatitis E virus infection
- hepatitis, fulminant viral, susceptibility to
- hepatitis, infectious canine
- hepatitis, non-human animal
- hepatitis, viral, animal
- hepatobiliary benign neoplasm
- hepatobiliary disorder
- hepatobiliary neoplasm
- hepatobiliary system
- hepatoblast
- hepatoblastoma
- hepatocellular adenoma
- hepatocellular carcinoma
- hepatocellular clear cell carcinoma
- hepatocellular fibrinogen storage disease, cattle
- hepatocellular fibrinogen storage disease, non-human animal
- hepatocyte
- hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
- hepatoerythropoietic porphyria
- hepatoid adenocarcinoma
- hepatopancreatic ampulla
- hepatoportal sclerosis
- hepatopulmonary syndrome
- hepatorenal syndrome
- hepatorenocardiac degenerative fibrosis
- hepatosplenic T-cell lymphoma
- hepatotoxic agent
- 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
- hereditary ataxia, non-human animal
- hereditary attention deficit-hyperactivity disorder
- hereditary benign intraepithelial dyskeratosis
