Mondo Disease Ontology
620 terms(s) returned
Term Type: Class | Record: 1 to 50 of 620 Records | Page: 1 of 13, First Previous Next Last | Show Records Per Page |
- G6PD deficiency
- GABA aminotransaminase deficiency
- GAPO syndrome
- GAPO syndrome, non-human animal
- GAPO syndrome, pig
- 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
- GCGR-related hyperglucagonemia
- GJC2-related late-onset primary lymphedema
- GLUT1 deficiency syndrome
- GM1 gangliosidosis
- GM1 gangliosidosis type 1
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM2 gangliosidosis
- GM3 synthase deficiency
- GMS syndrome
- GNAO1-related developmental delay-seizures-movement disorder spectrum
- GNAT2-related retinopathy
- GNE myopathy
- GNPTAB-mucolipidosis
- GNPTG-mucolipidosis
- GOMBO syndrome
- GPR143-related foveal hypoplasia
- GPR179-related retinopathy
- GRACILE syndrome
- GRFoma
- GRID2-related autosomal dominant spinocerebellar ataxia
- GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
- GRM6-related retinopathy
- 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
- Gaisbock syndrome
- Galloway-Mowat syndrome
- Galloway-Mowat syndrome 1
- Galloway-Mowat syndrome 10
- Galloway-Mowat syndrome 2, X-linked
- Galloway-Mowat syndrome 3
- Galloway-Mowat syndrome 4
- Galloway-Mowat syndrome 5
- Galloway-Mowat syndrome 6
- Galloway-Mowat syndrome 7