Experimental Factor Ontology
2823 terms(s) returned
| Term Type: | Record: 2701 to 2750 of 2823 Records | Page: 55 of 57, First Previous Next Last | Show Records Per Page |
- 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 9 with early respiratory failure
- myofibrillar myopathy, dominant
- myofibroblastoma
- myofibromatosis, infantile, 1
- myofibromatosis, infantile, 2
- myoglobin
- myoglobin measurement
- myoglobinuria, recurrent
- myomatous neoplasm
- myomesin-1
- myomesin-2
- myomesin-2 measurement
- myomesin-3
- myometrium
- myoneurin
- 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 of extraocular muscle
- myopathy with abnormal lipid metabolism
- myopathy with hexagonally cross-linked tubular arrays
- myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis
- myopathy, centronuclear, 2
- myopathy, centronuclear, 5
- myopathy, centronuclear, 6, with fiber-type disproportion
- 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 respiratory insufficiency and bone fractures
- myopathy, distal, 7, adult-onset, X-linked
- myopathy, epilepsy, and progressive cerebral atrophy
- myopathy, lactic acidosis, and sideroblastic anemia
