Experimental Factor Ontology
93744 terms(s) returned
| Term Type: | Record: 88801 to 88850 of 93744 Records | Page: 1777 of 1875, First Previous Next Last | Show Records Per Page |
- striatonigral degeneration
- striatonigral degeneration, childhood-onset
- striatonigral degeneration, infantile, mitochondrial
- stricture
- stricture or kinking of ureter
- stroke disorder
- stroke outcome severity measurement
- stroma of bone marrow
- stromal cell
- stromal cell of lamina propria of large intestine
- stromal cell of lamina propria of small intestine
- stromal cell-derived factor 1
- stromal cell-derived factor 1 (human)
- stromal cell-derived factor 1 alpha measurement
- stromal cell-derived factor 1 measurement
- stromal cell-derived factor 1 proteolytic cleavage product
- stromal cell-derived factor 1, signal peptide removed form (human)
- stromal cell-derived factor 2
- stromal cell-derived factor 2 (human)
- stromal cell-derived factor 2-like protein 1
- stromal cell-derived factor 2-like protein 1 (human)
- stromal cell-derived factor 2-like protein 1 measurement
- stromal corneal dystrophy
- stromal corneal pigmentation
- stromal interaction molecule 1
- stromal interaction molecule 1 (human)
- stromal interaction molecule 1 measurement
- stromal interaction molecule 1, signal peptide removed form (human)
- stromal membrane-associated protein 1
- stromal membrane-associated protein 1 (human)
- stromal membrane-associated protein 1 measurement
- stromal predominant kidney Wilms tumor
- stromelysin-1
- stromelysin-1 (human)
- stromelysin-1 proteolytic cleavage product
- stromelysin-1, signal peptide removed form (human)
- stromelysin-2
- stromelysin-2 (human)
- stromelysin-2 measurement
- stromelysin-2 proteolytic cleavage product
- stromelysin-2, signal peptide removed form (human)
- stromelysinâ1 measurement
- strongyloidiasis
- strontium atom
- strontium dichloride
- structural brain anomalies with impaired intellectual development and craniosynostosis
- structural congenital heart disease, multiple types - GATA4
- structural epilepsy
- structural heart defects and renal anomalies syndrome
- structural maintenance of chromosomes protein 3
