Mondo Disease Ontology
3925 terms(s) returned
| Term Type: | Record: 3751 to 3800 of 3925 Records | Page: 76 of 79, First Previous Next Last | Show Records Per Page |
- myoclonus, horse
- myoclonus, intractable, neonatal
- myoclonus, non-human animal
- myoclonus-cerebellar ataxia-deafness syndrome
- myoclonus-dystonia syndrome
- myocoele
- myocyte of atrioventricular node
- myocyte of sinoatrial node
- myoepithelial cell
- myoepithelial cell of bronchus submucosal gland
- myoepithelial cell of dilator pupillae
- myoepithelial cell of lactiferous alveolus
- myoepithelial cell of lactiferous duct
- myoepithelial cell of sweat gland
- myoepithelial cell of trachea gland
- myoepithelial tumor
- myoepithelium
- myofascial pain syndrome
- myofibril
- myofibrillar myopathy
- myofibrillar myopathy 1
- myofibrillar myopathy 10
- myofibrillar myopathy 11
- myofibrillar myopathy 2
- myofibrillar myopathy 3
- myofibrillar myopathy 4
- myofibrillar myopathy 5
- myofibrillar myopathy 6
- myofibrillar myopathy 7
- myofibrillar myopathy 8
- myofibrillar myopathy, horse
- myofibrillar myopathy, non-human animal
- myofibroblast cell
- myofibroblastoma
- myofibroma
- myofibromatosis, infantile, 1
- myofibromatosis, infantile, 2
- myofilament
- myoglobinuria, acute recurrent, autosomal recessive
- myoglobinuria, recurrent
- myomatous neoplasm
- myometrial cell
- myometrium
- myopathic intestinal pseudoobstruction
- myopathy
- myopathy caused by variation in CRPPA
- myopathy caused by variation in FKRP
- myopathy caused by variation in FKTN
- myopathy caused by variation in GMPPB
- myopathy caused by variation in POMGNT1
