Diseases — T

23 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.

• Tangier diseaseHOLD · ↓ DOWN · restore by supplyABCA1
• Tatton-Brown-Rahman overgrowth syndromeHOLD · ↓ DOWN · restore by supplyDNMT3A
• Tay-Sachs diseaseNOVEL · ↓ DOWN · restore by supplyHEXA
• TCF20 syndrome OMIM 618430HOLD · ↓ DOWN · restore by supplyTCF20
• TetrahydrobiopterinMATCH · ↓ DOWN · restore by supplyPTS
• Thanatophoric dysplasiaMATCH · ↑ UP · restore by clearFGFR3
• Trichohepatoenteric syndrome 1HOLD · ↓ DOWN · restore by supplyTTC37
• Thiamine-responsive megaloblastic anaemia / Rogers syndromeMATCH · ↓ DOWN · restore by supplySLC19A2
• Thrombocytopenia-absent radiusHOLD · ↓ DOWN · restore by supplyRBM8A
• Timothy syndromeNOVEL · ↑ UP · restore by clearCACNA1C
• TNF-receptor-associated periodic syndrome / TRAPSMATCH · ↑ UP · restore by clearTNFRSF1A
• Townes-BrocksHOLD · ↓ DOWN · restore by supplySALL1
• Triosephosphate isomerase deficiencyHOLD · ↓ DOWN · restore by supplyTPI1
• Transaldolase deficiencyHOLD · ↓ DOWN · restore by supplyTALDO1
• Transcobalamin II deficiencyMATCH · ↓ DOWN · restore by supplyTCN2
• Hereditary transthyretin amyloidosis OMIM 105210MATCH · ↓ DOWN · restore by clearTTR
• Treacher Collins syndrome 1HOLD · ↓ DOWN · restore by supplyTCOF1
• Trichothiodystrophy 1, photosensitiveHOLD · ↓ DOWN · restore by supplyERCC2
• Tuberous-like / mTORopathyMATCH · ↑ UP · restore by clearMTOR
• Tuberous sclerosis complex OMIM 191100MATCH · ↑ UP · restore by clearTSC2
• Tubulinopathy / lissencephaly 3HOLD · ↓ DOWN · restore by supplyTUBA1A
• Tufting enteropathyHOLD · ↓ DOWN · restore by supplyEPCAM
• Tyrosine hydroxylase deficiencyMATCH · ↓ DOWN · restore by supplyTH