Diseases — F
37 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.
- Fabry disease OMIM 301500MATCH · ↓ DOWN · restore by supplyGLA
- Factor V deficiencyMATCH · ↓ DOWN · restore by supplyF5
- Factor V Leiden thrombophiliaMATCH · ↑ UP · restore by clearF5
- Congenital factor VII deficiencyMATCH · ↓ DOWN · restore by supplyF7
- Factor X deficiencyMATCH · ↓ DOWN · restore by supplyF10
- Factor XI deficiencyMATCH · ↓ DOWN · restore by supplyF11
- Congenital factor XIII deficiencyMATCH · ↓ DOWN · restore by supplyF13A1
- Familial chylomicronaemia syndromeMATCH · ↑ UP · restore by clearLPL
- Familial dysautonomiaHOLD · ↓ DOWN · restore by supplyELP1
- Familial hemiplegic migraine 2HOLD · ↑ UP · restore by clearATP1A2
- Familial hypercholesterolaemia OMIM 143890MATCH · ↓ DOWN · restore by clearPCSK9
- Familial hypercholesterolemia type 1, LDL receptorMATCH · ↑ UP · restore by clearLDLR
- Familial Mediterranean feverMATCH · ↑ UP · restore by clearMEFV
- Familial TAADMATCH · ↑ UP · restore by clearACTA2
- Familial TAADMATCH · ↑ UP · restore by clearMYH11
- Familial TAADMATCH · ↑ UP · restore by clearTGFB2
- Fanconi anemia AMATCH · ↓ DOWN · restore by supplyFANCA
- Fanconi-BickelHOLD · ↓ DOWN · restore by supplySLC2A2
- Farber diseaseHOLD · ↑ UP · restore by clearASAH1
- Fructose-1,6-bisphosphatase deficiencyMATCH · ↓ DOWN · restore by supplyFBP1
- Familial cold autoinflammatoryMATCH · ↑ UP · restore by clearNLRP12
- FEVRHOLD · ↓ DOWN · restore by supplyFZD4
- FEVRHOLD · ↓ DOWN · restore by supplyLRP5
- Familial HLH 2MATCH · ↑ UP · restore by clearPRF1
- Familial hemophagocytic lymphohistiocytosisMATCH · ↑ UP · restore by clearUNC13D
- Familial hemophagocytic lymphohistiocytosisMATCH · ↑ UP · restore by clearSTX11
- Floating-Harbor syndromeHOLD · ↓ DOWN · restore by supplySRCAP
- Focal segmental GSHOLD · ↑ UP · restore by clearINF2
- Focal segmental GSHOLD · ↑ UP · restore by clearTRPC6
- FOXG1 syndrome OMIM 613454HOLD · ↓ DOWN · restore by supplyFOXG1
- FOXN1HOLD · ↓ DOWN · restore by supplyFOXN1
- FOXP1 syndrome OMIM 613670HOLD · ↓ DOWN · restore by supplyFOXP1
- Fraser syndromeHOLD · ↓ DOWN · restore by supplyFRAS1
- Friedreich ataxia OMIM 229300MATCH · ↓ DOWN · restore by supplyFXN
- FucosidosisHOLD · ↑ UP · restore by clearFUCA1
- Fukuyama CMDHOLD · ↓ DOWN · restore by supplyFKTN
- Fumarase deficiencyHOLD · ↑ UP · restore by clearFH