Diseases — G

44 diseases in this group. Each links to a full page: the emergence switch, the forced corrective direction, mapped agents, and the firewall. Direction only — no dose.

• GABRA1HOLD · ↓ DOWN · restore by supplyGABRA1
• GABRB3 encephalopathy OMIM 617113MATCH · ↓ DOWN · restore by supplyGABRB3
• GalactosialidosisHOLD · ↑ UP · restore by clearCTSA
• Galactokinase deficiencyMATCH · ↑ UP · restore by clearGALK1
• Guanidinoacetate methyltransferase deficiencyMATCH · ↓ DOWN · restore by supplyGAMT
• GATA2 deficiencyHOLD · ↓ DOWN · restore by supplyGATA2
• Gaucher disease OMIM 230800MATCH · ↓ DOWN · restore by supplyGBA1
• Gamma-glutamylcysteine synthetase deficiencyHOLD · ↓ DOWN · restore by supplyGCLC
• GEFS+HOLD · ↑ UP · restore by clearSCN1B
• Geroderma osteodysplasticaHOLD · ↓ DOWN · restore by supplyGORAB
• Giant axonal neuropathyHOLD · ↓ DOWN · restore by supplyGAN
• Gitelman syndromeMATCH · ↓ DOWN · restore by supplySLC12A3
• Glanzmann thrombastheniaMATCH · ↓ DOWN · restore by supplyITGA2B
• Glucose-6-phosphate dehydrogenase deficiencyMATCH · ↑ UP · restore by clearG6PD
• Glucose-galactose malabsorptionMATCH · ↓ DOWN · restore by supplySLC5A1
• GLUT1 deficiency syndrome / De Vivo diseaseMATCH · ↓ DOWN · restore by supplySLC2A1
• Glutaric aciduria 2-likeMATCH · ↓ DOWN · restore by supplyETFB
• Glutaric aciduria type 1MATCH · ↑ UP · restore by clearGCDH
• Glycerol kinase deficiencyHOLD · ↑ UP · restore by clearGK
• Glycine encephalopathyMATCH · ↑ UP · restore by clearAMT
• Glycogen storage disease type Ia / von Gierke diseaseMATCH · ↓ DOWN · restore by supplyG6PC1
• GM1 gangliosidosisHOLD · ↓ DOWN · restore by supplyGLB1
• GM2 gangliosidosis, AB variantHOLD · ↓ DOWN · restore by supplyGM2A
• GNAO1 encephalopathy OMIM 615473MATCH · ↑ UP · restore by clearGNAO1
• GNB1 encephalopathyHOLD · ↑ UP · restore by clearGNB1
• GNE myopathy / hereditary inclusion-body myopathyNOVEL · ↓ DOWN · restore by supplyGNE
• Gordon syndromeMATCH · ↑ UP · restore by clearWNK1
• Gorlin syndromeMATCH · ↑ UP · restore by clearPTCH1
• Glucose phosphate isomerase deficiencyHOLD · ↓ DOWN · restore by supplyGPI
• GRACILE syndromeHOLD · ↓ DOWN · restore by supplyBCS1L
• Gray platelet syndromeHOLD · ↓ DOWN · restore by supplyNBEAL2
• Greenberg dysplasiaHOLD · ↑ UP · restore by clearLBR
• GRIN1 encephalopathy OMIM 614254HOLD · ↓ DOWN · restore by supplyGRIN1
• GRIN2A epilepsy-aphasia OMIM 245570HOLD · ↑ UP · restore by clearGRIN2A
• GRIN2B encephalopathy OMIM 613970HOLD · ↓ DOWN · restore by supplyGRIN2B
• Griscelli syndrome type 2MATCH · ↑ UP · restore by clearRAB27A
• Glycogen storage disease IbMATCH · ↑ UP · restore by clearSLC37A4
• Glycogen storage disease IIIMATCH · ↓ DOWN · restore by supplyAGL
• McArdle diseaseMATCH · ↓ DOWN · restore by supplyPYGM
• Glycogen storage disease type VIMATCH · ↓ DOWN · restore by supplyPYGL
• Tarui diseaseHOLD · ↓ DOWN · restore by supplyPFKM
• GSD 0 muscleHOLD · ↓ DOWN · restore by supplyGYS1
• Glutathione synthetase deficiencyHOLD · ↓ DOWN · restore by supplyGSS
• Gyrate atrophy of the choroid and retinaMATCH · ↑ UP · restore by clearOAT