Experimental Factor Ontology
2464 terms(s) returned
| Term Type: | Record: 551 to 600 of 2464 Records | Page: 12 of 50, First Previous Next Last | Show Records Per Page |
- Hepadnaviridae infectious disease
- Hepatic Granuloma
- 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
- Hepatitis, Alcoholic
- Hepatobiliary Neoplasm
- Hepatoblastoma
- Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1
- Hepatoid Adenocarcinoma
- Hepatomegaly
- Hepatopulmonary Syndrome
- Hepatosplenomegaly
- 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
- Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
- Hereditary late-onset Parkinson disease
- Hereditary myoclonus - progressive distal muscular atrophy
- Hereditary orotic aciduria
- Hereditary persistence of alpha-fetoprotein
- Hereditary persistence of fetal hemoglobin - beta-thalassemia
- Hereditary proximal myopathy with early respiratory failure
- Hereditary vascular retinopathy
- Hermansky-Pudlak syndrome
- Hermansky-Pudlak syndrome 10
- Hermansky-Pudlak syndrome 11
- Hermansky-Pudlak syndrome 2
