Experimental Factor Ontology
4200 terms(s) returned
| Term Type: | Record: 4051 to 4100 of 4200 Records | Page: 82 of 84, First Previous Next Last | Show Records Per Page |
- myogenesis-regulating glycosidase (human)
- myoglobin
- myoglobin (human)
- myoglobin measurement
- myoglobin, initiator methionine removed form
- myoglobin, initiator methionine removed form (human)
- myoglobinuria, acute recurrent, autosomal recessive
- myoglobinuria, recurrent
- myomatous neoplasm
- myomesin-1
- myomesin-2
- myomesin-2 (human)
- myomesin-2 measurement
- myomesin-3
- myomesin-3 (human)
- myometrium
- myoneurin
- myoneurin (human)
- 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 1
- myopathy, autophagic vacuolar, infantile-onset
- 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, congenital, with structured cores and z-line abnormalities
- myopathy, congenital, with tremor
- myopathy, distal, 5
- myopathy, distal, 6, adult-onset, autosomal dominant
- myopathy, distal, 7, adult-onset, X-linked
- myopathy, epilepsy, and progressive cerebral atrophy
- myopathy, lactic acidosis, and sideroblastic anemia
- myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy
