Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 233 for neurological diseases
  1. PSAP gene 
    ... other organs. This accumulation results in very severe neurological disease, respiratory problems, and hepatosplenomegaly. Prosaposin (sphingolipid activator protein- ...
    https://medlineplus.gov/genetics/gene/psap - Genetics
  2. Deoxyguanosine kinase deficiency 
    ... a milder form of the disorder without severe neurological problems. Liver disease is the primary symptom of this form of the disorder, generally becoming evident during infancy or childhood. Occasionally it first ... of the disorder. ...
    https://medlineplus.gov/.../deoxyguanosine-kinase-deficiency - Genetics
  3. Aicardi-Goutières syndrome 
    ... I, Plebani A. Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? Autoimmun Rev. ...
    https://medlineplus.gov/.../condition/aicardi-goutieres-syndrome - Genetics
  4. HEPACAM gene 
    ... GlialCAM, a glial cell adhesion molecule implicated in neurological disease. Adv Neurobiol. 2014;8:47-59. doi: 10. ...
    https://medlineplus.gov/genetics/gene/hepacam - Genetics
  5. OPA1 gene 
    ... R, Amati-Bonneau P, Chinnery PF. Multi-system neurological disease is common in patients with OPA1 mutations. Brain. ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  6. SHANK3 gene 
    ... postsynaptic density with an emerging role in human neurological disease. J Neurochem. 2002 Jun;81(5):903-10. ...
    https://medlineplus.gov/genetics/gene/shank3 - Genetics
  7. ADAR gene 
    ... Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease. Neuropediatrics. 2017 Jun;48(3):166-184. doi: ...
    https://medlineplus.gov/genetics/gene/adar - Genetics
  8. MPV17-related hepatocerebral mitochondrial DNA depletion syndrome 
    ... is an inherited disorder that can cause liver disease and neurological problems. The signs and symptoms of this condition ... develop liver cancer. After the onset of liver disease, many affected infants develop neurological problems, which can include developmental delay, weak muscle ...
    https://medlineplus.gov/...bral-mitochondrial-dna-depletion-syndrome - Genetics
  9. PRNP gene 
    ... protein gene codon 129 modulates clinical course of neurological Wilson disease. Neuroreport. 2006 Apr 3;17(5):549-52. ... the human prion gene on the onset of neurological and hepatic symptoms in Wilson disease. Arch Neurol. 2006 Jul;63(7):982-5. ...
    https://medlineplus.gov/genetics/gene/prnp - Genetics
  10. Wilson disease 
    ... condition include a combination of liver disease and neurological and psychiatric problems.Liver disease is typically the initial feature of Wilson disease ...
    https://medlineplus.gov/genetics/condition/wilson-disease - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next