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Results 71 - 80 of 1,007 for Brain disorder
  1. Hereditary sensory and autonomic neuropathy type IE 
    ... DNMT1 are linked to a spectrum of neurological disorders. Brain. 2015 Apr;138(Pt 4):845-61. doi: 10.1093/brain/awv010. Epub 2015 Feb 11. Citation on PubMed or Free article on PubMed ... Citation on PubMed
    https://medlineplus.gov/...-sensory-and-autonomic-neuropathy-type-ie - Genetics
  2. GM2 activator deficiency 
    ... GM2 gangliosidosis, AB variant) is a rare inherited disorder that causes progressive brain injury. Most individuals with GM2 activator deficiency have ...
    https://medlineplus.gov/genetics/condition/gm2-activator-deficiency - Genetics
  3. TPM3 gene 
    ... type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders. Brain Dev. 2001 Aug;23(5):298-302. doi: ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  4. RANBP2 gene 
    ... 3 or IIAE3, is a rare type of brain disease (encephalopathy) that occurs following a viral infection such ...
    https://medlineplus.gov/genetics/gene/ranbp2 - Genetics
  5. Congenital fiber-type disproportion 
    ... type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders. Brain Dev. 2001 Aug;23(5):298-302. doi: ...
    https://medlineplus.gov/.../congenital-fiber-type-disproportion - Genetics
  6. Beta-propeller protein-associated neurodegeneration 
    ... protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation. Brain. 2013 Jun;136(Pt 6): ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  7. Leukoencephalopathy with vanishing white matter 
    ... is a progressive disorder that mainly affects the brain and spinal cord (central nervous system). This disorder causes deterioration of the central nervous system's ...
    https://medlineplus.gov/...ncephalopathy-with-vanishing-white-matter - Genetics
  8. Guanidinoacetate methyltransferase deficiency 
    ... is an inherited disorder that primarily affects the brain and muscles. Without early treatment, people with this disorder have neurological problems that are usually severe. These ...
    https://medlineplus.gov/...idinoacetate-methyltransferase-deficiency - Genetics
  9. Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 
    ... polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis. Am ...
    https://medlineplus.gov/...ogyria-polydactyly-hydrocephalus-syndrome - Genetics
  10. WDR45 gene 
    ... protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation. Brain. 2013 Jun;136(Pt 6): ...
    https://medlineplus.gov/genetics/gene/wdr45 - Genetics
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