Diseases — H
54 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.
- Hypomyelination with atrophy of the basal gangliaHOLD · ↓ DOWN · restore by supplyTUBB4A
- Haemophilia AMATCH · ↓ DOWN · restore by supplyF8
- Haemophilia BMATCH · ↓ DOWN · restore by supplyF9
- Hailey-HaileyHOLD · ↑ UP · restore by clearATP2C1
- Haploinsufficiency of A20MATCH · ↑ UP · restore by clearTNFAIP3
- Harlequin ichthyosisHOLD · ↓ DOWN · restore by supplyABCA12
- Hartnup disorderMATCH · ↓ DOWN · restore by supplySLC6A19
- HCMMATCH · ↑ UP · restore by clearACTC1
- Hypertrophic cardiomyopathyMATCH · ↑ UP · restore by clearMYBPC3
- HCMMATCH · ↑ UP · restore by clearMYL2
- HCMMATCH · ↑ UP · restore by clearTPM1
- HCN1 encephalopathy OMIM 615871HOLD · ↑ UP · restore by clearHCN1
- Hereditary coproporphyriaMATCH · ↑ UP · restore by clearCPOX
- Hemophagocytic LHMATCH · ↑ UP · restore by clearSTXBP2
- Hennekam lymphangiectasiaHOLD · ↓ DOWN · restore by supplyCCBE1
- Hereditary angioedemaMATCH · ↑ UP · restore by clearSERPING1
- Hereditary antithrombin deficiencyMATCH · ↑ UP · restore by clearSERPINC1
- Hereditary diffuse leukoencephHOLD · ↓ DOWN · restore by supplyCSF1R
- Hereditary elliptocytosisHOLD · ↓ DOWN · restore by supplyEPB41
- Hereditary folate malabsorptionMATCH · ↓ DOWN · restore by supplySLC46A1
- Hereditary fructose intoleranceMATCH · ↑ UP · restore by clearALDOB
- Hereditary haemochromatosis type 1MATCH · ↑ UP · restore by clearHFE
- Hereditary haemorrhagic telangiectasiaNOVEL · ↑ UP · restore by clearENG
- Hereditary pancreatitisHOLD · ↑ UP · restore by clearPRSS1
- Hereditary spastic ataxiaHOLD · ↑ UP · restore by clearKIF1A
- Hereditary spherocytosisMATCH · ↓ DOWN · restore by supplyANK1
- Hereditary spherocytosisMATCH · ↓ DOWN · restore by supplySPTB
- Hereditary tyrosinaemia type I OMIM 276700MATCH · ↑ UP · restore by clearFAH
- HeterotaxyHOLD · ↓ DOWN · restore by supplyZIC3
- Hoyeraal-HreidarssonMATCH · ↓ DOWN · restore by supplyTINF2
- Hyperinsulinism-hyperammonemiaMATCH · ↑ UP · restore by clearGLUD1
- Hidrotic ectodermal dysplasiaHOLD · ↑ UP · restore by clearGJB6
- Hexokinase deficiencyHOLD · ↓ DOWN · restore by supplyHK1
- HMG-CoA lyase deficiencyHOLD · ↑ UP · restore by clearHMGCL
- HNRNPUHOLD · ↓ DOWN · restore by supplyHNRNPU
- Holocarboxylase synthetase deficiencyMATCH · ↓ DOWN · restore by supplyHLCS
- HoloprosencephalyHOLD · ↓ DOWN · restore by supplySHH
- Holt-Oram syndromeHOLD · ↓ DOWN · restore by supplyTBX5
- Hermansky-Pudlak syndromeHOLD · ↓ DOWN · restore by supplyHPS1
- HSAN1NOVEL · ↑ UP · restore by clearSPTLC1
- Congenital insensitivity to pain with anhidrosisHOLD · ↓ DOWN · restore by supplyNTRK1
- Hereditary sensory and autonomic neuropathy type VHOLD · ↓ DOWN · restore by supplyNGF
- Hypomagnesemia with secondary hypocalcemiaMATCH · ↓ DOWN · restore by supplyTRPM6
- HSP 31HOLD · ↓ DOWN · restore by supplyREEP1
- HSP 5ANOVEL · ↑ UP · restore by clearCYP7B1
- Huntington disease OMIM 143100NOVEL · ↓ DOWN · restore by clearHTT
- Hereditary hyperekplexiaMATCH · ↑ UP · restore by clearGLRA1
- HyperekplexiaMATCH · ↓ DOWN · restore by supplySLC6A5
- Hyper-IgM syndromeMATCH · ↓ DOWN · restore by supplyCD40LG
- Hyperornithinaemia-hyperammonaemia-homocitrullinuriaMATCH · ↓ DOWN · restore by supplySLC25A15
- Hypertrophic cardiomyopathyMATCH · ↑ UP · restore by clearMYH7
- Familial hypomagnesemia with hypercalciuriaMATCH · ↓ DOWN · restore by supplyCLDN16
- Hypophosphatasia OMIM 241500MATCH · ↓ DOWN · restore by supplyALPL
- Hypokalemic periodic paralysis 1MATCH · ↑ UP · restore by clearCACNA1S