Mondo Disease Ontology
3949 terms(s) returned
| Term Type: | Record: 3801 to 3850 of 3949 Records | Page: 77 of 79, First Previous Next Last | Show Records Per Page |
- 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 of the diaphragmatic muscles, cattle
- myopathy of the diaphragmatic muscles, non-human animal
- 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 myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1
- myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2
- 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
- myopathy, congenital, progressive, with scoliosis
- myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies
- myopathy, congenital, with excess of muscle spindles
- myopathy, congenital, with fiber-type disproportion, X-linked
- myopathy, congenital, with respiratory insufficiency and bone fractures
