Center for Små Handicapgrupper er en selvejende institution underSocialministeriet og indgår i VISOs vidensfunktion under ServicestyrelsenCentret informerer og rådgiver både borgere og fagpersoner om sjældne handicap
Machado-Joseph sygdom
Madelungs deformitet
Maffucci syndrom
Makroglobulinæmi
Mandibulofacial dysostosis
Mannosidose
Maple syrup urine disease
Marfan syndrom
Maroteux-Lamy syndrom
MASA syndrom
Massiv osteolyse
Mastocytose
MCADD
McArdle sygdom
McCune-Albright syndrom
MEB syndrom
MECP2 duplikation syndrom
Medfødt Adrenal hyperplasi
Medfødt erytropoietisk porfyri
Medfødt hydronefrose
Medfødt hyperinsulinisme
Medfødt knogleskørhed
Medfødt nefrogen diabetes insipidus
Megacolon congenitum
Megalencephalic leukoencephalophathy
Meier-Gorlin syndrom
MELAS
Melkersson-Rosenthal syndrom
Mellemkædet acyl-CoA dehydrogenase defekt
Melnick-Needles syndrom
MEN
MEN1
MEN2
Meningocele
Menkes sygdom
Mental retardation - progressive spasticity, X-linked
Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs (MASA)
Mental retardation, X-linked, due to MECP2 duplication
MERRF
Metachondromatose
Metafysær dysostose
Metafysær kondrodysplasi, type Jansen
Metakromatisk leukodystrofi
Methylcrotonyl-CoA carboxylase defekt
Methylentetrahydrofolat reduktase defekt
Methylglutaconicaciduria
Methylglutaconsyreæmi
Methylmalonicaciduria
Methylmalonsyreæmi
Microtia-Anotia
Mikrocefalisk primordial dværgvækst
Mikroti
Milroy sygdom
Mitokondrie-sygdomme
Mitokondrielle encefalopatier
Mitokondrielle Myopatier
MLD
Monochromasi, blå
Monosomi 20p12
Monosomi 9p syndrom
Monosomy 22q11
Morbus Osler
Morbus Rendu-Weber-Osler
Morning glory syndrome
Morquio syndrom
Morris syndrom
Motor neuron disease
Mowat-Wilson syndrom
Moyamoya
Muckle-Wells syndrom
Mucopolysakkaridose
Mucopolysakkaridose I (Hurler syndrom)
Mucopolysakkaridose I (Hurler-Scheie syndrom)
Mucopolysakkaridose I (Scheie syndrom)
Mucopolysakkaridose II
Mucopolysakkaridose III
Mucopolysakkaridose IV
Mucopolysakkaridose VI
Muenke syndrom
Multifocal Fibrosclerosis
Multipel carboxylase mangel
Multipel endokrin neoplasi
Multipel endokrin neoplasi type 1
Multipel endokrin neoplasi type 2
Multipel epifysedysplasi
Multipel systematrofi
Multiple enchondromatosis
Multiple kartilaginøse exostoser
Muscle-Eye-Brain syndrom
Muskel fosforylase mangel
Myasthenic syndrom
Myelofibrose
Myelomeningocele
Myoclonic epilepsy with ragged red fibres
Myofosforylasemangel
Myopathy, encephalopathy, lactic acidosis and stroke-like episodes
Myositis ossificans progressiva
Myotubolære myopati
Möbius syndrom
