Experimental Factor Ontology
1774 terms(s) returned
| Term Type: | Record: 251 to 300 of 1774 Records | Page: 6 of 36, First Previous Next Last | Show Records Per Page |
- Ramsay-Hunt syndrome
- Ran GTPase-activating protein 1
- Ran-binding protein 3
- Ran-specific GTPase-activating protein
- Rana chensinensis
- Rana pirica
- Rap guanine nucleotide exchange factor 1
- Rap guanine nucleotide exchange factor 2
- Rap guanine nucleotide exchange factor 5
- Rap1 GTPase-GDP dissociation stimulator 1
- Rap1 GTPase-activating protein 1
- Rapid Amplification of cDNA Ends
- Rapid-onset childhood obesity - hypothalamic dysfunction - hypoventilation - autonomic dysregulation syndrome
- Rapid-onset dystonia-parkinsonism
- Rapture
- Rare bone disease related to a common gene or pathway defect
- Rare cataract
- Rare conjunctival disease
- Rare constitutional anemia
- Rare constitutional hemolytic anemia
- Rare constitutional hemolytic anemia due to a red cell membrane anomaly
- Rare constitutional hemolytic anemia due to an enzyme disorder
- Rare constitutional medullar aplasia
- Rare disease with autism
- Rare disease with corpus callosum agenesis associated with peripheral neuropathy
- Rare disease with dentinogenesis imperfecta
- Rare disease with glaucoma as a major feature
- Rare disease with thoracic aortic aneurysm and aortic dissection
- Rare disorder with dystonia and other neurologic or systemic manifestation
- Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism
- Rare disorder with hypergonadotropic hypogonadism
- Rare disorder with hypogonadotropic hypogonadism
- Rare dyslipidemia
- Rare eyebrow/eyelashes anomaly
- Rare familial disorder with hypertrophic cardiomyopathy
- Rare female infertility due to a congenital hypogonadotropic hypogonadism
- Rare female infertility due to adrenal disorder of genetic origin
- Rare female infertility due to an anomaly of ovarian function of genetic origin
- Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
- Rare genetic adrenal disease
- Rare genetic bone development disorder
- Rare genetic bone disease
- Rare genetic cardiac disease
- Rare genetic coagulation disorder
- Rare genetic deafness
- Rare genetic developmental defect during embryogenesis
- Rare genetic diabetes mellitus
- Rare genetic disease with myoclonus as a major feature
- Rare genetic disorder with obstructive azoospermia
- Rare genetic dystonia
