Mondo Disease Ontology
3651 terms(s) returned
Term Type: Class | Record: 3501 to 3550 of 3651 Records | Page: 71 of 74, First Previous Next Last | Show Records Per Page |
- 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
- myopathy caused by variation in POMGNT2
- myopathy caused by variation in POMT1
- myopathy caused by variation in POMT2
- myopathy due to calsequestrin and SERCA1 protein overload
- myopathy due to malate-aspartate shuttle defect
- myopathy due to myoadenylate deaminase deficiency
- myopathy of extraocular muscle
- myopathy with abnormal lipid metabolism
- myopathy with giant abnormal mitochondria
- myopathy with hexagonally cross-linked tubular arrays
- myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis
- myopathy with storage of glycoproteins and Glycosaminoglycans
- myopathy, autophagic vacuolar, infantile-onset
- myopathy, centronuclear, 2
- myopathy, centronuclear, 5
- myopathy, centronuclear, 6, with fiber-type disproportion
- myopathy, chicken
- myopathy, congenital proximal, with minicore lesions