Mondo Disease Ontology
3949 terms(s) returned
| Term Type: | Record: 2801 to 2850 of 3949 Records | Page: 57 of 79, First Previous Next Last | Show Records Per Page |
- mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency
- mitochondrial single-subunit type RNA polymerase binding
- mitochondrial substrate carrier disorder
- mitochondrial transcription
- mitochondrial transcription factor activity
- mitochondrial translation
- mitochondrial translational elongation
- mitochondrial translational initiation
- mitochondrial translational termination
- mitochondrial transmembrane transport
- mitochondrial transport
- mitochondrial trifunctional protein deficiency
- mitochondrial trifunctional protein deficiency 1
- mitochondrial trifunctional protein deficiency 2
- mitochondrion
- mitochondrion DNA recombination
- mitochondrion organization
- mitotic cell cycle
- mitotic cell cycle process
- mitotic chromosome condensation
- mitotic nuclear division
- mitotic sister chromatid segregation
- mitral atresia disorder
- mitral cell
- mitral valve
- mitral valve anulus
- mitral valve cusp
- mitral valve disease, dog
- mitral valve disease, non-human animal
- mitral valve disorder
- mitral valve dysplasia, ass
- mitral valve dysplasia, domestic cat
- mitral valve dysplasia, horse
- mitral valve dysplasia, non-human animal
- mitral valve insufficiency
- mitral valve leaflet
- mitral valve prolapse
- mitral valve prolapse, myxomatous 2
- mitral valve prolapse, myxomatous 3
- mitral valve stenosis
- mitral valve stenosis, domestic cat
- mitral valve stenosis, non-human animal
- mixed anxiety and depressive disorder
- mixed astrocytoma-ependymoma
- mixed astrocytoma-ependymoma-oligodendroglioma
- mixed cell adenoma
- mixed cell type adenoma of parathyroid
- mixed cell type kidney Wilms' tumor
- mixed cell uveal melanoma
- mixed cerebral palsy
