Human Disease Ontology
330 terms(s) returned
| Term Type: | Record: 1 to 50 of 330 Records | Page: 1 of 7, First Previous Next Last | Show Records Per Page |
- GABA aminotransferase deficiency
- GAND syndrome
- GAPO syndrome
- GM1 gangliosidosis
- GM1 gangliosidosis type 1
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM2 gangliosidosis
- GM2 gangliosidosis, AB variant
- GNE myopathy
- GOLD
- GRACILE syndrome
- GRID2-related spinocerebellar ataxia
- Galloway-Mowat syndrome
- Galloway-Mowat syndrome 1
- Galloway-Mowat syndrome 2
- Galloway-Mowat syndrome 3
- Galloway-Mowat syndrome 4
- Galloway-Mowat syndrome 5
- Gamstorp-Wohlfart syndrome
- Gasserian ganglion meningioma
- Gaucher's disease
- Gaucher's disease perinatal lethal
- Gaucher's disease type I
- Gaucher's disease type II
- Gaucher's disease type III
- Gaucher's disease type IIIC
- Gerstmann syndrome
- Gerstmann-Straussler-Scheinker syndrome
- Ghosal hematodiaphyseal syndrome
- Gilbert syndrome
- Gilles de la Tourette syndrome
- Gillespie syndrome
- Gitelman syndrome
- Glanzmann's thrombasthenia
- Goldberg-Shprintzen syndrome
- Goldenhar syndrome
- Good syndrome
- Goodpasture syndrome
- Gordon Holmes syndrome
- Gorham's disease
- Graves ophthalmopathy
- Graves' disease
- Greenberg dysplasia
- Greig cephalopolysyndactyly syndrome
- Griscelli syndrome
- Griscelli syndrome type 1
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
