Experimental Factor Ontology
114 terms(s) returned
| Term Type: | Record: 1 to 50 of 114 Records | Page: 1 of 3, First Previous Next Last | Show Records Per Page |
- HERNS syndrome
- HSD10 disease
- HSD10 disease, atypical type
- Hair defect - photosensitivity - intellectual disability
- Hallux varus - preaxial polysyndactyly
- Harlequin ichthyosis
- Hearing loss - familial salivary gland insensitivity to aldosterone
- Heart defect - round face - congenital developmental delay
- Heart defect-tongue hamartoma-polysyndactyly syndrome
- Heart defects - limb shortening
- Hematological disorder with renal involvement
- Hemihypertrophy
- Hemoglobin C - beta-thalassemia
- Hemoglobin E - beta-thalassemia
- Hemoglobin Lepore - beta-thalassemia
- 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
- Hepatic fibrosis - renal cysts - intellectual disability
- Hepatic veno-occlusive disease - immunodeficiency
- Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1
- 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 type 7
- Hermansky-Pudlak syndrome type 8
- Hermansky-Pudlak syndrome type 9
- Hermansky-Pudlak syndrome with neutropenia
