Mondo Disease Ontology
703 terms(s) returned
| Term Type: | Record: 1 to 50 of 703 Records | Page: 1 of 15, 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
- GBA1-related Parkinson disease, susceptibility
- GCGR-related hyperglucagonemia
- GJC2-related late-onset primary lymphedema
- GLUT1 deficiency syndrome
- GM1 gangliosidosis
- GM1 gangliosidosis GLB1-related, sheep
- GM1 gangliosidosis type 1
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM1 gangliosidosis, GLB1-related, dog
- GM1 gangliosidosis, GLB1-related, domestic cat
- GM1 gangliosidosis, cattle
- GM2 gangliosidosis
- GM2 gangliosidosis, GM2A-related, domestic cat
- GM2 gangliosidosis, HEXA-related, American flamingo
- GM2 gangliosidosis, HEXA-related, dog
- GM2 gangliosidosis, HEXA-related, pig
- GM2 gangliosidosis, HEXA-related, sheep
- GM2 gangliosidosis, HEXB-related dog
- GM2 gangliosidosis, HEXB-related, domestic cat
- GM2 gangliosidosis, Muntjak deer
- GM2 gangliosidosis, dog
- GM2 gangliosidosis, domestic cat
- GM2 gangliosidosis, pig
- GM2 gangliosidosis, rabbit
- GM2 gangliosidosis, springbok
- 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
