Experimental Factor Ontology
4252 terms(s) returned
| Term Type: | Record: 1251 to 1300 of 4252 Records | Page: 26 of 86, First Previous Next Last | Show Records Per Page |
- Microsporum ferrugineum
- Microsporum gallinae
- Microtia - eye coloboma - imperforation of the nasolacrimal duct
- Middle East reference superpopulation (HGDP)
- Middle East respiratory syndrome
- Middle cerebral artery stenosis
- Midface retrusion
- Midline defect of mandible
- Midline facial cleft
- Mietens syndrome
- Mijikenda
- Mikati-Najjar-Sahli syndrome
- Mild conductive hearing impairment
- Mild expressive language delay
- Mild fetal ventriculomegaly
- Mild global developmental delay
- Mild hearing impairment
- Mild intellectual disability
- Mild malformation of cortical development
- Mild microcephaly
- Mild proteinuria
- Mild short stature
- Mildly elevated creatine kinase
- Miller Fisher syndrome
- Miller-Dieker lissencephaly syndrome
- Miller-Dieker syndrome
- Milroy disease
- Mimulus guttatus
- Mini-International Neuropsychiatric Interview
- Minianka
- Minicore myopathy
- Mint-ChIP
- Miosis
- Mirror image polydactyly
- Mirror polydactyly - vertebral segmentation - limbs defects
- Miscanthus x giganteus
- Miscarriage
- Miscellaneous movement disorder due to genetic neurodegenerative disease
- Missing ribs
- Mitchell syndrome
- MitoRCA-seq
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
- Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
- Mitochondrial disease with dilated cardiomyopathy
- Mitochondrial disease with eye involvement
- Mitochondrial disease with hypertrophic cardiomyopathy
- Mitochondrial disease with peripheral neuropathy
- Mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes
- Mitochondrial disorder due to a defect in mitochondrial protein synthesis
