Experimental Factor Ontology
3087 terms(s) returned
| Term Type: | Record: 801 to 850 of 3087 Records | Page: 17 of 62, First Previous Next Last | Show Records Per Page |
- Hemolytic anemia due to a disorder of glycolytic enzymes
- Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder
- Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
- Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies
- Hemolytic anemia due to red cell pyruvate kinase deficiency
- Hemophagocytosis
- Hemoptysis
- Hengel-Maroofian-Schols syndrome
- Hennekam lymphangiectasia-lymphedema syndrome 2
- Hennekam syndrome
- Hennekam-Beemer syndrome
- Henoch-Schoenlein purpura
- Hep3B
- HepG2
- HepG3
- Hepa 1-6
- HepaRG
- Hepadnaviridae infectious disease
- Hepatic cysts
- Hepatic failure
- Hepatic fibrosis
- Hepatic fibrosis - renal cysts - intellectual disability
- Hepatic hemangioma
- Hepatic necrosis
- Hepatic steatosis
- Hepatic veno-occlusive disease - immunodeficiency
- Hepatitis
- Hepatitis B virus core antigen seropositivity
- Hepatitis B virus surface antigen seropositivity
- Hepatitis C virus
- Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1
- Hepatomegaly
- Hepatosplenomegaly
- Her2-receptor negative breast cancer
- Herbaspirillum seropedicae SmR1
- Hereditary breast and ovarian cancer syndrome
- Hereditary breast cancer
- Hereditary central diabetes insipidus
- Hereditary cerebral hemorrhage with amyloidosis
- Hereditary cerebral hemorrhage with amyloidosis, Arctic type
- Hereditary cerebral hemorrhage with amyloidosis, Dutch type
- Hereditary cerebral hemorrhage with amyloidosis, Flemish type
- Hereditary cerebral hemorrhage with amyloidosis, Icelandic type
- Hereditary cerebral hemorrhage with amyloidosis, Iowa type
- Hereditary cerebral hemorrhage with amyloidosis, Italian type
- Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
- Hereditary combined deficiency of vitamin K-dependent clotting factors
- Hereditary cryohydrocytosis with normal stomatin
- Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia
- Hereditary epidermolysis bullosa associated with ocular features
