Experimental Factor Ontology
315 terms(s) returned
| Term Type: | Record: 1 to 50 of 315 Records | Page: 1 of 7, First Previous Next Last | Show Records Per Page |
- GABA aminotransaminase deficiency
- GAPO syndrome
- GATA1-Related X-Linked Cytopenia
- GATA2 deficiency with susceptibility to MDS/AML
- GATA5-related congenital heart defects
- GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes
- GBA1-related Parkinson disease, susceptibility
- GCGR-related hyperglucagonemia
- GLUT1 deficiency syndrome
- GM1 gangliosidosis
- GM1 gangliosidosis type 1
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM2 gangliosidosis
- GM3 synthase deficiency
- GMS syndrome
- GNE myopathy
- GNPTAB-mucolipidosis
- GNPTG-mucolipidosis
- GPR143-related foveal hypoplasia
- GRACILE syndrome
- GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
- GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
- GTP cyclohydrolase I deficiency
- GTP cyclohydrolase I deficiency with hyperphenylalaninemia
- GUCY2D retinopathy
- GUCY2D-related dominant retinopathy
- GUCY2D-related recessive retinopathy
- GYG1-related disorder of glycogen metabolism
- Gabriele de Vries syndrome
- Galloway-Mowat syndrome
- Galloway-Mowat syndrome 10
- Galloway-Mowat syndrome 2, X-linked
- Galloway-Mowat syndrome 9
- Gamstorp-Wohlfart syndrome
- Gardner syndrome
- Garg-Mishra progeroid syndrome
- Gaucher disease
- Gaucher disease due to saposin C deficiency
- Gaucher disease perinatal lethal
- Gaucher disease type I
- Gaucher disease type II
- Gaucher disease type III
- Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
- German syndrome
- Gerstmann-Straussler-Scheinker syndrome
- Gitelman syndrome
- Glanzmann thrombasthenia
- Glanzmann thrombasthenia 1
- Goldberg-Shprintzen syndrome
