Experimental Factor Ontology
620 terms(s) returned
| Term Type: | Record: 151 to 200 of 620 Records | Page: 4 of 13, First Previous Next Last | Show Records Per Page |
- immunodeficiency, common variable, 7
- immunodeficiency, developmental delay, and hypohomocysteinemia
- immunodeficiency-centromeric instability-facial anomalies syndrome
- immunodeficiency-related disorder
- immunoglobulin heavy chain deficiency
- immunoglobulin-mediated membranoproliferative glomerulonephritis
- immunoproliferative disorder
- immunoskeletal dysplasia with neurodevelopmental abnormalities
- impaired renal function disease
- imperforate anus
- imperforate oropharynx-costo vetebral anomalies syndrome
- impulse control disorder
- in situ carcinoma
- inborn aminoacylase deficiency
- inborn carbohydrate metabolic disorder
- inborn disorder of amino acid and other organic acid metabolism
- inborn disorder of amino acid metabolism
- inborn disorder of amino acid transport
- inborn disorder of aspartate family metabolism
- inborn disorder of bile acid synthesis
- inborn disorder of bilirubin metabolism
- inborn disorder of biogenic amine metabolism and transport
- inborn disorder of branched-chain amino acid metabolism
- inborn disorder of cobalamin metabolism and transport
- inborn disorder of energy metabolism
- inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation
- inborn disorder of histidine metabolism
- inborn disorder of ketolysis
- inborn disorder of lysine and hydroxylysine metabolism
- inborn disorder of lysosomal amino acid transport
- inborn disorder of methionine cycle and sulfur amino acid metabolism
- inborn disorder of neurotransmitter metabolism and transport
- inborn disorder of ornithine metabolism
- inborn disorder of ornithine or proline metabolism
- inborn disorder of pentose phosphate metabolism
- inborn disorder of peptide metabolism
- inborn disorder of phenylalanine and tyrosine metabolism
- inborn disorder of porphyrin metabolism
- inborn disorder of proline metabolism
- inborn disorder of purine metabolism
- inborn disorder of purine or pyrimidine metabolism
- inborn disorder of pyridoxine metabolism
- inborn disorder of pyrimidine metabolism
- inborn disorder of serine family metabolism
- inborn disorder of the gamma-glutamyl cycle
- inborn disorder of tryptophan metabolism
- inborn error of biotin metabolism
- inborn error of immunity
- inborn errors of metabolism
- inborn glycerol kinase deficiency
