BioAssay Ontology
261 terms(s) returned
| Term Type: | Record: 51 to 100 of 261 Records | Page: 2 of 6, First Previous Next Last | Show Records Per Page |
- Fox-Fordyce disease
- Frasier syndrome
- Frey syndrome
- Friedreich ataxia
- FuGENE 6
- Fuchs' endothelial dystrophy
- Fuchs' heterochromic uveitis
- Fukuyama congenital muscular dystrophy
- fMLFF peptide
- fMLFK-FITC
- facial dermatosis
- facial hemiatrophy
- facial nerve disease
- facial paralysis
- facioscapulohumeral muscular dystrophy
- factor V deficiency
- factor VII deficiency
- factor VIII deficiency
- factor X deficiency
- factor XI deficiency
- factor XII deficiency
- factor XIII deficiency
- fallopian tube adenocarcinoma
- fallopian tube cancer
- fallopian tube carcinoma
- fallopian tube disease
- familial Mediterranean fever
- familial adenomatous polyposis
- familial atrial fibrillation
- familial chylomicronemia syndrome
- familial combined hyperlipidemia
- familial hyperlipidemia
- familial juvenile hyperuricemic nephropathy
- familial lipoprotein lipase deficiency
- familial medullary thyroid carcinoma
- familial melanoma
- familial periodic paralysis
- familial retinoblastoma
- farmer's lung
- farnesoid X receptor agonist
- fasciculated
- fasciculated axons phenotype
- fasciitis
- fascioliasis
- fasciolopsiasis
- fat-soluble vitamin
- fatal familial insomnia
- fatty acid catabolic process
- fatty acid oxidation inhibitor
- fatty acid synthesis inhibitor
