Mondo Disease Ontology
3933 terms(s) returned
| Term Type: | Record: 2201 to 2250 of 3933 Records | Page: 45 of 79, First Previous Next Last | Show Records Per Page |
- methemoglobinemia, CYB5R3-related, domestic cat
- methemoglobinemia, alpha type
- methemoglobinemia, domestic cat
- methemoglobinemia, non-human animal
- methicillin-resistant staphylococcus aureus infectious disease
- methicillin-susceptible staphylococcus aureus infectious disease
- methimazole embryofetopathy
- methionine adenosyltransferase deficiency
- methionine malabsorption syndrome
- methionine metabolic process
- methotrexate
- methotrexate toxicity
- methotrexate(1-)
- methotrexate(2-)
- methotrexate-associated lymphoproliferative disorders
- methoxide
- methyl ester
- methyl transfer-driven active transmembrane transporter activity
- methylamine metabolic process
- methylation
- methylbenzene
- methylcobalamin deficiency type cblDv1
- methylcobalamin deficiency type cblE
- methylcobalamin deficiency type cblG
- methylcrotonoyl-CoA carboxylase activity
- methylmalonate semialdehyde dehydrogenase deficiency
- methylmalonate(1-)
- methylmalonate(2-)
- methylmalonic acid
- methylmalonic acidemia
- methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
- methylmalonic acidemia due to transcobalamin receptor defect
- methylmalonic acidemia with homocystinuria, type cblJ
- methylmalonic acidemia with homocystinuria, type cblX
- methylmalonic aciduria and homocystinuria
- methylmalonic aciduria and homocystinuria type cblC
- methylmalonic aciduria and homocystinuria type cblD
- methylmalonic aciduria and homocystinuria type cblF
- methylmalonic aciduria and homocystinuria, cb1L type
- methylmalonic aciduria and/or homocystinuria, cblD type
- methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
- methylmalonic aciduria, cblA type
- methylmalonic aciduria, cblB type
- methylpyridines
- methyltransferase activity
- mevalonate kinase deficiency
- mevalonic aciduria
- miRNA_encoding
- miRNA_gene
- microangiopathy and leukoencephalopathy, pontine, autosomal dominant
