Mondo Disease Ontology
2149 terms(s) returned
| Term Type: | Record: 801 to 850 of 2149 Records | Page: 17 of 43, First Previous Next Last | Show Records Per Page |
- imperforate hymen, cattle
- imperforate hymen, horse
- imperforate oropharynx-costo vetebral anomalies syndrome
- impetigo
- impetigo herpetiformis
- implicit_genetic_in_ordo
- import into cell
- import ontology module
- imported from
- imprinting gene related to retinoblastoma
- impulse control disorder
- impulsive behavior
- in branch
- in branching relationship with
- in situ carcinoma
- in taxon
- in utero embryonic development
- in_innermost_side_of
- in_subset
- inappropriate ADH syndrome
- 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 glutamate/glutamine and aspartate/asparagine metabolism
- inborn disorder of glycine and serine 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 lysine, hydroxylysine, and tryptophan 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 ornithine, proline and hydroxyproline 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
