Experimental Factor Ontology
4252 terms(s) returned
| Term Type: | Record: 1901 to 1950 of 4252 Records | Page: 39 of 86, First Previous Next Last | Show Records Per Page |
- manic episode measurement
- manic or hypomanic episode
- mannan-binding lectin serine protease 1
- mannan-binding lectin serine protease 1 (human)
- mannan-binding lectin serine protease 1 amount
- mannan-binding lectin serine protease 1 proteolytic cleavage product
- mannan-binding lectin serine protease 1, signal peptide removed form
- mannan-binding lectin serine protease 1, signal peptide removed form (human)
- mannitol
- mannitol measurement
- mannonate
- mannonate measurement
- mannose
- mannose measurement
- mannose-1-phosphate guanylyltransferase regulatory subunit alpha
- mannose-1-phosphate guanylyltransferase regulatory subunit alpha (human)
- mannose-1-phosphate guanylyltransferase regulatory subunit alpha amount in blood
- mannose-6-phosphate isomerase
- mannose-6-phosphate isomerase (human)
- mannose-binding lectin deficiency
- mannose-binding protein C
- mannose-binding protein C (human)
- mannose-binding protein C measurement
- mannose-binding protein C, signal peptide removed form
- mannose-binding protein C, signal peptide removed form (human)
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IA
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IA (human)
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IA measurement
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IB
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IB (human)
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IB measurement
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IC
- mannosyl-oligosaccharide 1,2-alpha-mannosidase IC (human)
- mansonelliasis
- mantle cell
- mantle cell lymphoma
- manus
- map kinase p38
- maple syrup urine disease
- maple syrup urine disease type 1A
- maple syrup urine disease type 1B
- maple syrup urine disease type 2
- maple syrup urine disease, mild variant
- mapping_justification
- marasmus
- marcothrombocytopenia with mitral valve insufficiency
- marfan syndrome/loeys-dietz syndrome/familial thoracic aortic aneurysms and dissections
- marfanoid habitus and intellectual disability
- marfanoid habitus-autosomal recessive intellectual disability syndrome
- marfanoid habitus-inguinal hernia-advanced bone age syndrome
