Diseases — B

32 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.

• B4GALT1-CDGHOLD · ↓ DOWN · restore by supplyB4GALT1
• Bainbridge-Ropers syndromeHOLD · ↓ DOWN · restore by supplyASXL3
• Bardet-Biedl syndrome 2MATCH · ↓ DOWN · restore by supplyBBS2
• Bardet-Biedl syndrome 4MATCH · ↓ DOWN · restore by supplyBBS4
• Bardet-Biedl syndrome 7MATCH · ↓ DOWN · restore by supplyBBS7
• Bardet-Biedl syndrome 9MATCH · ↓ DOWN · restore by supplyBBS9
• Bardet-Biedl syndromeMATCH · ↓ DOWN · restore by supplyBBS1
• Bardet-Biedl syndrome 10MATCH · ↓ DOWN · restore by supplyBBS10
• Barth syndromeHOLD · ↓ DOWN · restore by supplyTAFAZZIN
• Bartter syndrome type 3HOLD · ↓ DOWN · restore by supplyCLCNKB
• Bartter syndrome type 1MATCH · ↓ DOWN · restore by supplySLC12A1
• Benign familial neonatal epilepsyMATCH · ↑ UP · restore by clearKCNQ3
• Bernard-Soulier syndromeHOLD · ↓ DOWN · restore by supplyGP1BA
• Best vitelliform dystrophyHOLD · ↓ DOWN · restore by supplyBEST1
• Beta-ketothiolase deficiencyMATCH · ↑ UP · restore by clearACAT1
• Beta-thalassaemiaMATCH · ↓ DOWN · restore by supplyHBB
• Bethlem myopathyHOLD · ↓ DOWN · restore by supplyCOL6A3
• Collagen VI-related myopathyHOLD · ↓ DOWN · restore by supplyCOL6A2
• Biotin-thiamine-responsive basal ganglia diseaseMATCH · ↓ DOWN · restore by supplySLC19A3
• Biotinidase deficiency OMIM 253260MATCH · ↓ DOWN · restore by supplyBTD
• Birt-Hogg-Dube syndromeHOLD · ↑ UP · restore by clearFLCN
• Blau syndrome / early-onset sarcoidosisMATCH · ↑ UP · restore by clearNOD2
• Blepharophimosis-ptosis-epicanthus inversus syndromeHOLD · ↓ DOWN · restore by supplyFOXL2
• Bloom syndromeHOLD · ↓ DOWN · restore by supplyBLM
• Bohring-Opitz syndromeHOLD · ↓ DOWN · restore by supplyASXL1
• Branchio-oto-renal syndrome 1HOLD · ↓ DOWN · restore by supplyEYA1
• Bothnia retinal dystrophyHOLD · ↓ DOWN · restore by supplyRLBP1
• Beta-propeller protein-associated neurodegeneration / BPANHOLD · ↑ UP · restore by clearWDR45
• GDF5-related chondrodysplasia / brachydactylyHOLD · ↓ DOWN · restore by supplyGDF5
• Primary familial brain calcification 1HOLD · ↑ UP · restore by clearSLC20A2
• Brugada syndromeMATCH · ↓ DOWN · restore by clearSCN5A
• Brown-Vialetto-Van Laere syndrome 2MATCH · ↓ DOWN · restore by supplySLC52A2