Mondo Disease Ontology
4355 terms(s) returned
| Term Type: | Record: 2501 to 2550 of 4355 Records | Page: 51 of 88, First Previous Next Last | Show Records Per Page |
- 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
- methylmalonic-coA mutase deficiency, MMUT-related, sheep
- methylpyridines
- methyltransferase activity
- metritis, non-human animal
- mevalonate kinase deficiency
- mevalonic aciduria
- miRNA_encoding
- miRNA_gene
- microangiopathy and leukoencephalopathy, pontine, autosomal dominant
- microbial food material
- microbial/enzymatic modification process
- microbody
- microbrachycephaly-ptosis-cleft lip syndrome
- microcephalic osteodysplastic dysplasia, Saul-Wilson type
- microcephalic osteodysplastic primordial dwarfism
- microcephalic osteodysplastic primordial dwarfism type I
- microcephalic osteodysplastic primordial dwarfism type II
- microcephalic osteodysplastic primordial dwarfism types I and III
- microcephalic osteodysplastic primordial dwarfism, type 3
- microcephalic primordial dwarfism due to RTTN deficiency
