Mondo Disease Ontology
2169 terms(s) returned
| Term Type: | Record: 851 to 900 of 2169 Records | Page: 18 of 44, First Previous Next Last | Show Records Per Page |
- 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
- 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 the metabolism of sulfur-containing amino acids and hydrogen sulfide
- inborn disorder of tryptophan metabolism
- inborn error of biotin metabolism
- inborn error of hepatic metabolism, dog
- inborn error of hepatic metabolism, non-human animal
- inborn error of immunity
- inborn errors of metabolism
- inborn errors of metabolism, non-human animal
- inborn glycerol kinase deficiency
- inborn metal metabolism disorder
- inborn mitochondrial metabolism disorder
- inborn mitochondrial myopathy
- inborn organic aciduria
- inborn serine deficiency
- inborn vitamin metabolic disorder
- incessant infant ventricular tachycardia
- incisors, lower central, absence of
- incisors, rotation of upper central
- incisors, shovel-shaped
- inclusion body
- inclusion body myopathy and brain white matter abnormalities
- inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
- inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2
- inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
- inclusion body myositis
- inclusion compound
