Mondo Disease Ontology
4355 terms(s) returned
| Term Type: | Record: 2901 to 2950 of 4355 Records | Page: 59 of 88, First Previous Next Last | Show Records Per Page |
- mineralized bone tissue
- mineralized extracellular matrix
- mineralized skeletal tissue
- mineralocorticoid
- mineralocorticoid biosynthetic process
- mineralocorticoid metabolic process
- mineralocorticoid secreting cell
- mineralocorticoid secretion
- minimal change disease
- minimal pigment oculocutaneous albinism type 1
- minimally invasive lung adenocarcinoma
- mink viral enteritis
- minor salivary gland
- minor salivary gland adenocarcinoma
- minor salivary gland adenoid cystic carcinoma
- minor salivary gland carcinoma
- minor vestibular gland
- minor vestibular glands adenoma
- miosis, dog
- mirror agnosia
- 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
- mirror-image polydactyly
- misaligned with
- misalliance, non-human animal
- mislocalised
- mislocalised posteriorly
- mismatch repair cancer syndrome
- mismatch repair cancer syndrome 1
- mismatch repair cancer syndrome 2
- mismatch repair cancer syndrome 3
- mismatch repair cancer syndrome 4
- missing tooth/teeth dental disorder, non-human animal
- mite infestation
- mites parasite infection, non-human animal
- 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 14B (cardioencephalomyopathic type)
- mitochondrial DNA depletion syndrome 15 (hepatocerebral type)
- mitochondrial DNA depletion syndrome 16 (hepatic type)
- mitochondrial DNA depletion syndrome 17
