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Results 1 - 10 of 2,633 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. OSMR gene 
    ... provides instructions for making a protein called oncostatin M receptor beta subunit (OSMRβ). This protein is one piece (subunit) of both the oncostatin M (OSM) receptor type II and the interleukin-31 ( ...
    https://medlineplus.gov/genetics/gene/osmr - Genetics
  4. TRPM1 gene 
    ... protein called transient receptor potential cation channel subfamily M member 1 (TRPM1). This protein acts as a ... 1 MLSN1 transient receptor potential cation channel, subfamily M, member 1 transient receptor potential melastatin family TRPM1_ ...
    https://medlineplus.gov/genetics/gene/trpm1 - Genetics
  5. TRPM4 gene 
    ... protein called transient receptor potential cation channel subfamily M member 4 (TRPM4). This protein acts as a ... melastatin-4 transient receptor potential cation channel, subfamily M, member 4 TRPM4_HUMAN TRPM4B Tests of TRPM4 ...
    https://medlineplus.gov/genetics/gene/trpm4 - Genetics
  6. 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
  7. MPLKIP gene 
    ... C7orf11) provides instructions for making a protein called M-phase specific PLK1 interacting protein. Based on its ... protein TTDN1 TTDN1_HUMAN Tests of MPLKIP PubMed M-PHASE-SPECIFIC PLK1-INTERACTING PROTEIN; MPLKIP NCBI Gene ...
    https://medlineplus.gov/genetics/gene/mplkip - Genetics
  8. TRPM6 gene 
    ... channel 6 transient receptor potential cation channel, subfamily M, member 6 Tests of TRPM6 PubMed TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY M, MEMBER 6; TRPM6 NCBI Gene ClinVar Chubanov V, ...
    https://medlineplus.gov/genetics/gene/trpm6 - Genetics
  9. LDHA gene 
    ... Condition L-lactate dehydrogenase A chain lactate dehydrogenase M LDH muscle subunit LDH-A LDH-M LDH1 LDHA_HUMAN LDHM Tests of LDHA PubMed ... A; LDHA NCBI Gene ClinVar Kanno T, Maekawa M. Lactate dehydrogenase M-subunit deficiencies: clinical features, metabolic ...
    https://medlineplus.gov/genetics/gene/ldha - Genetics
  10. PGAM2 gene 
    ... 2 GSD10 MGC88743 muscle-specific phosphoglycerate mutase PGAM-M PGAM2_HUMAN PGAMM phosphoglycerate mutase 2 (muscle) phosphoglycerate mutase isozyme M Tests of PGAM2 PubMed PHOSPHOGLYCERATE MUTASE 2; PGAM2 ...
    https://medlineplus.gov/genetics/gene/pgam2 - Genetics
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