A–Z DIRECTORY
Conditions beginning with G
- GABA-transaminase deficiencyAutosomal recessive
- GalactosemiaAutosomal recessive
- GalactosialidosisAutosomal recessive
- Gastrointestinal stromal tumorAutosomal dominant · Autosomal recessive
- Gaucher diseaseAutosomal recessive
- Geleophysic dysplasiaAutosomal recessive · Autosomal dominant, or a new variant
- Generalized arterial calcification of infancyAutosomal recessive
- Generalized pustular psoriasisAutosomal recessive · Autosomal dominant
- Genetic epilepsy with febrile seizures plusAutosomal dominant
- Genitopatellar syndromeAutosomal dominant
- Gestational diabetesPattern unknown
- Ghosal hematodiaphyseal dysplasiaAutosomal recessive
- Giant axonal neuropathyAutosomal recessive
- Giant congenital melanocytic nevusNot inherited
- Gilbert syndromeAutosomal dominant · Autosomal recessive
- Gillespie syndromeAutosomal recessive · Autosomal dominant
- Gitelman syndromeAutosomal recessive
- Glanzmann thrombastheniaAutosomal recessive
- GlobozoospermiaAutosomal recessive
- Glucose phosphate isomerase deficiencyAutosomal recessive
- Glucose-6-phosphate dehydrogenase deficiencyX-linked
- Glucose-galactose malabsorptionAutosomal recessive
- GLUT1 deficiency syndromeAutosomal dominant · Autosomal recessive
- Glutamate formiminotransferase deficiencyAutosomal recessive
- Glutaric acidemia type IAutosomal recessive
- Glutaric acidemia type IIAutosomal recessive
- Glutathione synthetase deficiencyAutosomal recessive
- Glycogen storage disease type 0Autosomal recessive
- Glycogen storage disease type IAutosomal recessive
- Glycogen storage disease type IIIAutosomal recessive
- Glycogen storage disease type IVAutosomal recessive
- Glycogen storage disease type IXX-linked recessive · Autosomal recessive
- Glycogen storage disease type VAutosomal recessive
- Glycogen storage disease type VIAutosomal recessive
- Glycogen storage disease type VIIAutosomal recessive
- Glycoprotein VI deficiencyAutosomal recessive
- GM1 gangliosidosisAutosomal recessive
- GM2 activator deficiencyAutosomal recessive
- GM3 synthase deficiencyAutosomal recessive
- Gnathodiaphyseal dysplasiaAutosomal dominant
- GNE myopathyAutosomal recessive
- Gordon Holmes syndromeAutosomal recessive
- Gorlin syndromeAutosomal dominant
- Gorlin-Chaudhry-Moss syndromeAutosomal dominant
- GoutPattern unknown
- GRACILE syndromeAutosomal recessive
- Grange syndromeAutosomal recessive
- Granulomatosis with polyangiitisPattern unknown
- Graves' diseasePattern unknown
- Gray platelet syndromeAutosomal recessive · Autosomal dominant
- Greenberg dysplasiaAutosomal recessive
- Greig cephalopolysyndactyly syndromeAutosomal dominant
- GRIN2B-related neurodevelopmental disorderAutosomal dominant
- Griscelli syndromeAutosomal recessive
- GRN-related frontotemporal lobar degenerationAutosomal dominant
- Guanidinoacetate methyltransferase deficiencyAutosomal recessive
- Guillain-Barré syndromePattern unknown
- Gyrate atrophy of the choroid and retinaAutosomal recessive
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