Experimental Factor Ontology
12089 terms(s) returned
Term Type: | Record: 51 to 100 of 12089 Records | Page: 2 of 242, First Previous Next Last | Show Records Per Page |
- 3-methylcrotonyl-CoA carboxylase deficiency
- 3-methylglutaconic aciduria
- 3-methylglutaconic aciduria type 1
- 3-methylglutaconic aciduria type 3
- 3-methylglutaconic aciduria type 4
- 3-methylglutaconic aciduria type 5
- 3-methylglutaconic aciduria type 8
- 3-methylglutaconic aciduria type 9
- 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
- 3-methylglutaconic aciduria, type VIIB
- 3-phosphoglycerate dehydrogenase deficiency
- 3MC syndrome
- 3p- syndrome
- 3q26 microduplication syndrome
- 3q26q27 microdeletion syndrome
- 3q27.3 microdeletion syndrome
- 45,X/46,XY mixed gonadal dysgenesis
- 46 XX gonadal dysgenesis
- 46,XX disorder of sex development
- 46,XX disorder of sex development-anorectal anomalies syndrome
- 46,XX disorder of sex development-skeletal anomalies syndrome
- 46,XX ovotesticular disorder of sex development
- 46,XX sex reversal 1
- 46,XX testicular disorder of sex development
- 46,XY complete gonadal dysgenesis
- 46,XY disorder of sex development
- 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
- 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome
- 46,XY ovotesticular disorder of sex development
- 46,XY partial gonadal dysgenesis
- 46,XY sex reversal 1
- 46,XY sex reversal 3
- 46,XY sex reversal 4
- 46,XY sex reversal 6
- 46,xx sex reversal 5
- 47,XYY syndrome
- 48,XXXY syndrome
- 48,XXYY syndrome
- 48,XYYY syndrome
- 49,XXXXY syndrome
- 49,XXXYY syndrome
- 49,XYYYY syndrome
- 4p16.3 microduplication syndrome
- 5-oxoprolinase deficiency
- 5q14.3 microdeletion syndrome
- 5q35 microduplication syndrome
- 6-phosphogluconate dehydrogenase deficiency
- 6p22 microdeletion syndrome
- 6q terminal deletion syndrome