Diagnoselist
Show the list in following languagesen
Diagnoses, M
- Macrocephaly-Cutis Marmorata Telangiectatica Congenita (English)
- Macroglobulinemia, Waldenstrom (English)
- Macular Degeneration, Juvenile (English)
- Madelung deformity (English)
- Malignant hyperthermia (English)
- Mannosidosis, Alpha B, Lysosomal (English)
- Maple syrup urine disease, MSUD (English)
- Marfan syndrome (English)
- Marie-Strumpell spondylitis (English)
- Marinesco-Sjogren syndrome (English)
- Marker chromosome 11;22 (English)
- Marker chromosome 15 syndrome, Idic (15) syndrome, Isodicentric 15 syndrome, Inverted duplication (15) (English)
- Maroteaux-Lamy syndrome (English)
- Marshall-Smith syndrome (English)
- MASA syndrome (English)
- Mastocytosis (English)
- McArdle disease (English)
- McCune-Albright Syndrome (English)
- MEB (English)
- Medium-Chain Acyl-CoA Dehydrogenation Disorder (English)
- Megalencephalic Leukoencephalopathy With Subcortical Cysts (English)
- Meier-Gorlin Syndrome (English)
- MELAS (English)
- Melnick-Frasers Syndrome (English)
- Melnick-Needles syndrome (English)
- Menkes disease (English)
- Mental retardation, X-linked, due to MECP2 duplication (English)
- MERRF (English)
- Metachondromatosis (English)
- Metachromatic leukodystrophy (English)
- Metaphyseal Chondrodysplasia, Jansen Type (English)
- Methylenetetrahydrofolate Reductase Deficiency (English)
- Methylmalonic acidemia (English)
- Meyenburg-Altherr-Uehlinger Syndrome (English)
- Mikrotia (English)
- Mitochondrial Diseases (English)
- Mitochondrial myopathy, encephalopathy, lactid acidoses and stroke-like episodes (English)
- Mitochondrial Neurogastrointestinal Encephalopathy Syndrome (English)
- Moebius syndrome, Möbius sequence (English)
- Monosomy 13q syndrome, 13q deletion syndrome (English)
- Monosomy 18p (English)
- Monosomy 18q (English)
- Monosomy 1p36 (English)
- Monosomy 20p12 syndrome (English)
- Monosomy 4p (English)
- Monosomy 4q (English)
- Monosomy 9p syndrome (English)
- Morquio syndrome (English)
- Mosaic Trisomy 14 Syndrome (English)
- Mowat-Wilson syndrome (English)
- Moyamoya Disease (English)
- MRXSL (English)
- Muckle-Wells Syndrome (English)
- Mucocutaneous Lymph Node Syndrome (English)
- Mucolipidosis II (English)
- Mucopolysaccharidosis type I (IH, IH/S, IS); MPS I (IH, IH/S, IS) (English)
- Mucopolysaccharidosis type I H/S (English)
- Mucopolysaccharidosis type I S (English)
- Mucopolysaccharidosis type II, MPS II, Iduronate sulfatase deficiency (English)
- Mucopolysaccharidosis type III, MPS III (English)
- Mucopolysaccharidosis type IV (English)
- Mucopolysaccharidosis type VI (English)
- Mucopolysaccharidosis type VII (English)
- Muenke Syndrome (English)
- Mulibrey nanism (English)
- Multifocal motor neuropathy (English)
- Multiple Carboxylase Deficiency, Late-Onset (English)
- Multiple endocrine neoplasia type 2 (English)
- Multiple epiphyseal dysplasia, MED (English)
- Muscle-Eye-Brain Disease (English)
- Myelofibrosis (English)
- Myoclonic Epilepsy Associated With Ragged-Red Fibers (English)
- Myoclonic epilepsy of Lafora (English)
- Myoclonic Epilepsy Of Unverricht And Lundborg (English)
- Myopathy, centronuclear (English)
- Möbius syndrome (English)
Information
The information and descriptions of diagnoses is found through links to external pages (outside rarelink)
A diagnoses can be listed under several names, in both english and nordic languages.
