Experimental Factor Ontology
4222 terms(s) returned
| Term Type: | Record: 3051 to 3100 of 4222 Records | Page: 62 of 85, First Previous Next Last | Show Records Per Page |
- mimecan (human)
- mimecan, signal peptide removed form
- mineral metabolism disease
- mineralocorticoid receptor
- mineralocorticoid receptor (human)
- mineralocorticoid receptor measurement
- miniARS-seq
- minigene splicing assay
- minimal erythema dose
- minimal pigment oculocutaneous albinism type 1
- minimally invasive lung adenocarcinoma
- minocycline
- minor histocompatibility congenic strain
- minor salivary gland
- minor salivary gland adenocarcinoma
- minor salivary gland adenoid cystic carcinoma
- minor salivary gland carcinoma
- minosaminomycin measurement
- minute
- miotic rate
- mirror movements 1
- mirror movements 1 and/or agenesis of the corpus callosum
- mirror movements 2
- mirror movements 3
- mirror movements 4
- mirror polydactyly-vertebral segmentation-limbs defects syndrome
- mismatch repair cancer syndrome
- mismatch repair cancer syndrome 1
- mismatch repair endonuclease PMS2
- mismatch repair endonuclease PMS2 (human)
- mismatch repair endonuclease PMS2 measurement
- misshapen-like kinase 1
- mite infestation
- mitochondrial DNA
- mitochondrial DNA deletion syndrome with progressive myopathy
- mitochondrial DNA depletion syndrome
- mitochondrial DNA depletion syndrome 1
- mitochondrial DNA depletion syndrome 11
- mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant
- mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive
- mitochondrial DNA depletion syndrome 13
- mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)
- mitochondrial DNA depletion syndrome 15 (hepatocerebral type)
- mitochondrial DNA depletion syndrome 16 (hepatic type)
- mitochondrial DNA depletion syndrome 17
- mitochondrial DNA depletion syndrome 18
- mitochondrial DNA depletion syndrome 19
- mitochondrial DNA depletion syndrome 20 (mngie type)
- mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
- mitochondrial DNA depletion syndrome 4a
