Experimental Factor Ontology
692 terms(s) returned
Term Type: | Record: 151 to 200 of 692 Records | Page: 4 of 14, First Previous Next Last | Show Records Per Page |
- hemoglobin M disease
- hemoglobinopathy
- hemoglobinopathy Toms River
- hemoglobinuria
- hemolytic anemia due to adenylate kinase deficiency
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- hemolytic anemia due to glucophosphate isomerase deficiency
- hemolytic anemia due to glutathione reductase deficiency
- hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
- hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature
- hemolytic uremic syndrome, atypical, susceptibility to, 1
- hemolytic-uremic syndrome
- hemophagocytic lymphohistiocytosis, familial, 6
- hemophagocytic syndrome
- hemophilia
- hemophilia A
- hemophilia B
- hemorrhagic cystitis
- hemorrhagic disease
- hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
- hemorrhagic duodenitis
- hemorrhagic fever
- hemosiderosis
- heparin cofactor 2 deficiency
- hepatic angiomyolipoma
- hepatic fibrosis-renal cysts-intellectual disability syndrome
- hepatic porphyria
- hepatic vascular disorder
- hepatic veno-occlusive disease
- hepatic veno-occlusive disease-immunodeficiency syndrome
- hepatitis B virus, susceptibility to
- hepatitis C virus, susceptibility to
- hepatitis, fulminant viral, susceptibility to
- hepatobiliary benign neoplasm
- hepatocellular clear cell carcinoma
- hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
- hepatoerythropoietic porphyria
- hepatorenal syndrome
- hepatorenocardiac degenerative fibrosis
- hepatosplenic T-cell lymphoma
- hereditary North American Indian childhood cirrhosis
- hereditary Wilms tumor
- hereditary acrokeratotic poikiloderma, Weary type
- hereditary amyloidosis
- hereditary angioedema
- hereditary angioedema type 1
- hereditary angioedema type 2
- hereditary angioedema type 3
- hereditary angioedema with C1Inh deficiency