Diseases — C
111 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.
- Complement C1q deficiencyHOLD · ↓ DOWN · restore by supplyC1QA
- Complement C3 deficiencyHOLD · ↓ DOWN · restore by supplyC3
- Carnitine-acylcarnitine translocase deficiencyMATCH · ↓ DOWN · restore by supplySLC25A20
- CADASILHOLD · ↑ UP · restore by clearNOTCH3
- Campomelic dysplasiaHOLD · ↓ DOWN · restore by supplySOX9
- Congenital amegakaryocytic thrombocytopeniaMATCH · ↓ DOWN · restore by supplyMPL
- Camurati-Engelmann diseaseMATCH · ↑ UP · restore by clearTGFB1
- Canavan diseaseHOLD · ↑ UP · restore by clearASPA
- Proteasome-associated autoinflammatory syndrome / CANDLEMATCH · ↑ UP · restore by clearPSMB8
- Cantu syndromeMATCH · ↑ UP · restore by clearABCC9
- Cardiofaciocutaneous syndromeHOLD · ↑ UP · restore by clearMAP2K1
- Cartilage-hair hypoplasiaHOLD · ↓ DOWN · restore by supplyRMRP
- CASK-related disorder / MICPCHHOLD · ↓ DOWN · restore by supplyCASK
- Catecholaminergic polymorphic ventricular tachycardiaMATCH · ↑ UP · restore by clearRYR2
- CCDC115-CDG OMIM 616828HOLD · ↓ DOWN · restore by supplyCCDC115
- Congenital dyserythropoietic anemia type IHOLD · ↓ DOWN · restore by supplyCDAN1
- Congenital dyserythropoietic anemia type II / HEMPASHOLD · ↓ DOWN · restore by supplySEC23B
- Congenital dyserythropoietic anemiaHOLD · ↓ DOWN · restore by supplyKIF23
- Cranioectodermal dysplasiaHOLD · ↓ DOWN · restore by supplyWDR35
- Central core diseaseHOLD · ↓ DOWN · restore by supplyRYR1
- Autosomal recessive centronuclear myopathyHOLD · ↓ DOWN · restore by supplyBIN1
- Autosomal dominant centronuclear myopathyHOLD · ↑ UP · restore by clearDNM2
- Congenital erythropoietic porphyriaMATCH · ↑ UP · restore by clearUROS
- Cerebral folate transport deficiencyMATCH · ↓ DOWN · restore by supplyFOLR1
- Cerebrotendinous xanthomatosisMATCH · ↓ DOWN · restore by supplyCYP27A1
- Cardiofaciocutaneous syndromeHOLD · ↑ UP · restore by clearBRAF
- Chronic granulomatous disease XMATCH · ↓ DOWN · restore by supplyCYBB
- Chronic granulomatous diseaseMATCH · ↓ DOWN · restore by supplyNCF1
- Congenital generalized lipodystrophyMATCH · ↓ DOWN · restore by supplyAGPAT2
- Congenital generalized lipodystrophyMATCH · ↓ DOWN · restore by supplyBSCL2
- Chanarin-DorfmanHOLD · ↑ UP · restore by clearABHD5
- CHARGE syndromeHOLD · ↓ DOWN · restore by supplyCHD7
- CHD2 developmental and epileptic encephalopathyHOLD · ↓ DOWN · restore by supplyCHD2
- Chediak-HigashiHOLD · ↓ DOWN · restore by supplyLYST
- CherubismHOLD · ↑ UP · restore by clearSH3BP2
- ChoroideremiaNOVEL · ↓ DOWN · restore by supplyCHM
- Christianson syndromeHOLD · ↓ DOWN · restore by supplySLC9A6
- Congenital insensitivity to painHOLD · ↓ DOWN · restore by supplySCN9A
- Citrin deficiencyMATCH · ↓ DOWN · restore by supplySLC25A13
- Citrullinemia type 1MATCH · ↑ UP · restore by clearASS1
- Classic EDSHOLD · ↓ DOWN · restore by supplyCOL5A1
- Classic galactosaemiaMATCH · ↑ UP · restore by clearGALT
- Classical homocystinuriaMATCH · ↓ DOWN · restore by supplyCBS
- Cleidocranial dysplasiaHOLD · ↓ DOWN · restore by supplyRUNX2
- NCL1 infantileHOLD · ↓ DOWN · restore by supplyPPT1
- NCL3 juvenile BattenHOLD · ↑ UP · restore by clearCLN3
- Neuronal ceroid lipofuscinosisHOLD · ↓ DOWN · restore by supplyCLN5
- Neuronal ceroid lipofuscinosisHOLD · ↓ DOWN · restore by supplyCLN6
- Neuronal ceroid lipofuscinosisHOLD · ↓ DOWN · restore by supplyMFSD8
- Neuronal ceroid lipofuscinosisHOLD · ↓ DOWN · restore by supplyCLN8
- Congenital myasthenic syndromeMATCH · ↓ DOWN · restore by supplyCHAT
- CMSMATCH · ↓ DOWN · restore by supplyCHRNE
- Congenital myasthenic syndromeMATCH · ↓ DOWN · restore by supplyCOLQ
- Congenital myasthenic syndromeMATCH · ↓ DOWN · restore by supplyDOK7
- Congenital myasthenic syndrome with tubular aggregatesMATCH · ↓ DOWN · restore by supplyGFPT1
- Congenital myasthenic syndromeMATCH · ↓ DOWN · restore by supplyRAPSN
- CMT1BHOLD · ↓ DOWN · restore by supplyMPZ
- Charcot-Marie-Tooth disease 2DHOLD · ↓ DOWN · restore by supplyGARS1
- Charcot-Marie-Tooth disease 2EHOLD · ↓ DOWN · restore by supplyNEFL
- CMT 2AHOLD · ↓ DOWN · restore by supplyMFN2
- Charcot-Marie-Tooth disease 2F / distal HMNHOLD · ↓ DOWN · restore by supplyHSPB1
- Charcot-Marie-Tooth disease 2L / distal HMNHOLD · ↓ DOWN · restore by supplyHSPB8
- CMT 4HOLD · ↓ DOWN · restore by supplyGDAP1
- Charcot-Marie-Tooth disease 4CHOLD · ↓ DOWN · restore by supplySH3TC2
- Charcot-Marie-Tooth disease 4JHOLD · ↓ DOWN · restore by supplyFIG4
- CMT XHOLD · ↓ DOWN · restore by supplyGJB1
- Congenital nephrotic syndrome FinnishMATCH · ↑ UP · restore by clearNPHS1
- Methylmalonic aciduria and homocystinuria, cblC typeMATCH · ↓ DOWN · restore by supplyMMACHC
- Cockayne syndrome BHOLD · ↓ DOWN · restore by supplyERCC6
- Coffin-Lowry syndromeHOLD · ↓ DOWN · restore by supplyRPS6KA3
- Coffin-Siris syndromeHOLD · ↓ DOWN · restore by supplyARID1B
- Cohen syndromeHOLD · ↓ DOWN · restore by supplyVPS13B
- Combined deficiency of factor V and factor VIIIHOLD · ↓ DOWN · restore by supplyLMAN1
- Complement component 2 deficiencyMATCH · ↓ DOWN · restore by supplyC2
- Cone dystrophy with supernormal rod responseHOLD · ↓ DOWN · restore by supplyKCNV2
- Cone-rod dystrophyHOLD · ↓ DOWN · restore by supplyCRX
- Congenital adrenal hyperplasia, 21-hydroxylase deficiencyMATCH · ↓ DOWN · restore by supplyCYP21A2
- X-linked adrenal hypoplasia congenitaMATCH · ↓ DOWN · restore by supplyNR0B1
- Congenital cataractHOLD · ↓ DOWN · restore by supplyCRYAA
- Congenital chloride diarrheaMATCH · ↓ DOWN · restore by supplySLC26A3
- Congenital contractural arachnodactyly / Beals syndromeHOLD · ↓ DOWN · restore by supplyFBN2
- Congenital fibrosis of the extraocular muscles type 1HOLD · ↑ UP · restore by clearKIF21A
- Primary congenital glaucomaMATCH · ↑ UP · restore by clearCYP1B1
- Congenital hyperinsulinismMATCH · ↓ DOWN · restore by supplyKCNJ11
- Congenital hyperinsulinismMATCH · ↑ UP · restore by clearABCC8
- Congenital hypothyroidism, thyroglobulin defectMATCH · ↓ DOWN · restore by supplyTG
- Congenital hypothyroidism, thyroid peroxidase defectMATCH · ↓ DOWN · restore by supplyTPO
- Congenital leptin deficiency OMIM 614962MATCH · ↓ DOWN · restore by supplyLEP
- Congenital lipoid adrenal hyperplasiaMATCH · ↓ DOWN · restore by supplySTAR
- Conradi-HunermannHOLD · ↑ UP · restore by clearEBP
- Primary coenzyme Q10 deficiencyMATCH · ↓ DOWN · restore by supplyCOQ2
- Coenzyme Q10 deficiencyMATCH · ↓ DOWN · restore by supplyCOQ8A
- Cornelia de Lange syndromeHOLD · ↓ DOWN · restore by supplyNIPBL
- Cornelia de Lange 2HOLD · ↓ DOWN · restore by supplySMC1A
- Costello syndromeHOLD · ↑ UP · restore by clearHRAS
- Cowden syndromeMATCH · ↑ UP · restore by clearPTEN
- Carbamoyl phosphate synthetase I deficiencyMATCH · ↑ UP · restore by clearCPS1
- Carnitine palmitoyltransferase IA deficiencyMATCH · ↓ DOWN · restore by supplyCPT1A
- Carnitine palmitoyltransferase II deficiency, myopathicMATCH · ↓ DOWN · restore by supplyCPT2
- Catecholaminergic polymorphic ventricular tachycardiaMATCH · ↑ UP · restore by clearCASQ2
- Creatine transporter deficiencyHOLD · ↓ DOWN · restore by supplySLC6A8
- Crigler-Najjar syndrome 1MATCH · ↑ UP · restore by clearUGT1A1
- Crouzon syndromeNOVEL · ↓ DOWN · restore by clearFGFR2
- Cryopyrin-associated periodic syndromeMATCH · ↑ UP · restore by clearNLRP3
- CTLA4 haploinsufficiency / CHAIMATCH · ↓ DOWN · restore by supplyCTLA4
- CTNNB1 neurodevelopmental disorderHOLD · ↓ DOWN · restore by supplyCTNNB1
- Cutis laxaHOLD · ↓ DOWN · restore by supplyATP6V0A2
- Cutis laxaHOLD · ↓ DOWN · restore by supplyFBLN5
- Cystic fibrosis OMIM 219700MATCH · ↓ DOWN · restore by supplyCFTR
- CystinosisMATCH · ↑ UP · restore by clearCTNS
- CystinuriaMATCH · ↑ UP · restore by clearSLC7A9