Diseases — M
63 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.
- Glutaric aciduria type II / multiple acyl-CoA dehydrogenase…HOLD · ↓ DOWN · restore by supplyETFA
- Majeed syndromeHOLD · ↓ DOWN · restore by supplyLPIN2
- Mal de MeledaMATCH · ↑ UP · restore by clearSLURP1
- Mannosidosis betaHOLD · ↓ DOWN · restore by supplyMANBA
- Maple syrup urine diseaseMATCH · ↓ DOWN · restore by supplyBCKDHA
- Marfan syndromeMATCH · ↓ DOWN · restore by clearFBN1
- Marinesco-Sjogren syndromeHOLD · ↓ DOWN · restore by supplySIL1
- Maturity-onset diabetesMATCH · ↓ DOWN · restore by supplyHNF1A
- MBD5 neurodevelopmental OMIM 156200HOLD · ↓ DOWN · restore by supplyMBD5
- Meckel-Gruber syndrome type 1HOLD · ↓ DOWN · restore by supplyMKS1
- MECP2 duplication syndrome OMIM 300260NOVEL · ↑ UP · restore by clearMECP2
- MED13L syndrome OMIM 616789HOLD · ↓ DOWN · restore by supplyMED13L
- Medium-chain acyl-CoA dehydrogenase deficiencyMATCH · ↓ DOWN · restore by supplyACADM
- MEF2C haploinsufficiency syndromeHOLD · ↓ DOWN · restore by supplyMEF2C
- Megaconial congenital muscular dystrophyHOLD · ↓ DOWN · restore by supplyCHKB
- Megalencephalic leukoencephalopathy with subcortical cystsHOLD · ↓ DOWN · restore by supplyMLC1
- Megalencephaly-capillary malfMATCH · ↑ UP · restore by clearPIK3CA
- Menkes diseaseMATCH · ↓ DOWN · restore by supplyATP7A
- Merosin-deficient congenital muscular dystrophy 1AHOLD · ↓ DOWN · restore by supplyLAMA2
- Metachromatic leukodystrophyMATCH · ↓ DOWN · restore by supplyARSA
- Metatropic dysplasiaHOLD · ↑ UP · restore by clearTRPV4
- Methylmalonic acidaemiaMATCH · ↓ DOWN · restore by supplyMMUT
- Mevalonic aciduria / mevalonate kinase deficiencyMATCH · ↑ UP · restore by clearMVK
- 3-methylglutaconic aciduria type IHOLD · ↓ DOWN · restore by supplyAUH
- MHC class II deficiency / bare lymphocyte syndromeHOLD · ↓ DOWN · restore by supplyRFXANK
- Autosomal recessive primary microcephaly 5HOLD · ↓ DOWN · restore by supplyASPM
- Syndromic microphthalmia type 3HOLD · ↓ DOWN · restore by supplySOX2
- Milroy disease / primary congenital lymphoedemaHOLD · ↓ DOWN · restore by supplyFLT4
- McKusick-Kaufman syndromeHOLD · ↓ DOWN · restore by supplyMKKS
- MNGIE / mitochondrial neurogastrointestinal encephalomyopathyHOLD · ↓ DOWN · restore by supplyTYMP
- Molybdenum cofactor deficiency type BHOLD · ↓ DOWN · restore by supplyMOCS2
- Molybdenum cofactor deficiency type AMATCH · ↓ DOWN · restore by supplyMOCS1
- Mowat-Wilson syndromeHOLD · ↓ DOWN · restore by supplyZEB2
- Mitochondrial-membrane-protein-associated neurodegenerationHOLD · ↓ DOWN · restore by supplyC19ORF12
- MPI-CDG OMIM 602579MATCH · ↓ DOWN · restore by supplyMPI
- Mendelian susceptibility to mycobacterial diseaseHOLD · ↓ DOWN · restore by supplyIFNGR1
- Mucolipidosis II alpha/betaHOLD · ↓ DOWN · restore by supplyGNPTAB
- Mucolipidosis III gammaHOLD · ↓ DOWN · restore by supplyGNPTG
- Mucolipidosis IVHOLD · ↓ DOWN · restore by supplyMCOLN1
- Mucopolysaccharidosis type IMATCH · ↓ DOWN · restore by supplyIDUA
- Mucopolysaccharidosis type IIMATCH · ↓ DOWN · restore by supplyIDS
- Mucopolysaccharidosis type IIIANOVEL · ↓ DOWN · restore by supplySGSH
- Mucopolysaccharidosis type IIIBNOVEL · ↓ DOWN · restore by supplyNAGLU
- Mucopolysaccharidosis type IIICNOVEL · ↓ DOWN · restore by supplyHGSNAT
- Mucopolysaccharidosis type IIIDHOLD · ↓ DOWN · restore by supplyGNS
- Mucopolysaccharidosis type IVAMATCH · ↓ DOWN · restore by supplyGALNS
- Mucopolysaccharidosis type VIMATCH · ↓ DOWN · restore by supplyARSB
- Mucopolysaccharidosis type VIIMATCH · ↓ DOWN · restore by supplyGUSB
- Muenke syndromeNOVEL · ↑ UP · restore by clearFGFR3
- Multiminicore disease / SELENON-related myopathyHOLD · ↓ DOWN · restore by supplySELENON
- Multiple endocrine neoplasia 1MATCH · ↑ UP · restore by clearMEN1
- Multiple endocrine neoplasia type 2AMATCH · ↑ UP · restore by clearRET
- Multiple epiphyseal dysplasiaHOLD · ↓ DOWN · restore by supplyMATN3
- Multiple osteochondromasHOLD · ↓ DOWN · restore by supplyEXT1
- Multiple osteochondromasHOLD · ↓ DOWN · restore by supplyEXT2
- Multiple sulfatase deficiencyHOLD · ↓ DOWN · restore by supplySUMF1
- Microvillus inclusion diseaseHOLD · ↓ DOWN · restore by supplyMYO5B
- MYH9-related disorder OMIM 155100HOLD · ↑ UP · restore by clearMYH9
- Myofibrillar myopathyHOLD · ↓ DOWN · restore by supplyCRYAB
- Myofibrillar myopathyHOLD · ↓ DOWN · restore by supplyDES
- Myofibrillar myopathyHOLD · ↓ DOWN · restore by supplyFLNC
- Myofibrillar myopathyHOLD · ↓ DOWN · restore by supplyMYOT
- Myotonia congenitaMATCH · ↓ DOWN · restore by clearCLCN1