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Results 1 - 10 of 1,190 for ms
  1. 3-M syndrome 
    3-M syndrome is a disorder that causes skeletal abnormalities including short stature (dwarfism) and unusual facial features. The name of this condition ...
    https://medlineplus.gov/genetics/condition/3-m-syndrome - Genetics
  2. Multiple sclerosis 
    Multiple sclerosis is a condition characterized by areas of damage (lesions) on the brain and spinal cord. These ...
    https://medlineplus.gov/genetics/condition/multiple-sclerosis - Genetics
  3. Neuromyelitis optica 
    ... condition described in Japanese patients as optic-spinal multiple sclerosis (or opticospinal multiple sclerosis) that affects the nerves of the eyes and ...
    https://medlineplus.gov/genetics/condition/neuromyelitis-optica - Genetics
  4. Marinesco-Sjögren syndrome 
    ... Hereditary oligophrenic cerebello-lental degeneration Marinesco-Garland syndrome MSS Genetic Testing Registry: Marinesco-Sjögren syndrome Marinesco-Sjögren ...
    https://medlineplus.gov/.../condition/marinesco-sjogren-syndrome - Genetics
  5. Methemoglobinemia, beta-globin type 
    ... the disorder. Blue baby syndrome Congenital methemoglobinemia Hemoglobin M disease Genetic Testing Registry: Methemoglobinemia, beta-globin type Hemoglobin M disease National Organization for Rare Disorders (NORD) ClinicalTrials. ...
    https://medlineplus.gov/.../methemoglobinemia-beta-globin-type - Genetics
  6. Megalencephaly-capillary malformation syndrome 
    ... without a genetic mutation is known as mosaicism. M-CM Macrocephaly cutis marmorata telangiectatica congenita Macrocephaly-capillary ... V, Romanelli V, Mori MA, Gracia R, Segovia M, Gonzalez-Meneses A, Lopez-Gutierrez JC, Gean E, ...
    https://medlineplus.gov/...encephaly-capillary-malformation-syndrome - Genetics
  7. 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... 3-alpha-hydroxyacyl-CoA dehydrogenase, short chain, deficiency M/SCHAD deficiency SCHAD deficiency Genetic Testing Registry: Deficiency ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  8. VEXAS syndrome 
    ... L, Oda H, Goodspeed W, Barron KS, Nehrebecky M, Jones A, Laird RS, Deuitch N, Rowczenio D, ... E, Wells KV, Lee CR, Wang W, Trick M, Mullikin J, Wigerblad G, Brooks S, Dell'Orso ...
    https://medlineplus.gov/genetics/condition/vexas-syndrome - Genetics
  9. CUL3-related neurodevelopmental disorder 
    ... PubMed Blackburn PR, Ebstein F, Hsieh TC, Motta M, Radio FC, Herkert JC, Rinne T, Thiffault I, Rapp M, Alders M, Maas S, Gerard B, Smol T, Vincent-Delorme ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  10. KCNB1 encephalopathy 
    ... 26; DEE26 PubMed Bar C, Barcia G, Jennesson M, Le Guyader G, Schneider A, Mignot C, Lesca G, Breuillard D, Montomoli M, Keren B, Doummar D, Billette de Villemeur T, ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
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