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 47 for Mental disorders
  1. FBN1 gene 
    ... Bennetts B. FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited. Am J Med Genet A. 2006 May ...
    https://medlineplus.gov/genetics/gene/fbn1 - Genetics
  2. FMR1 gene 
    ... sensation in the lower extremities (peripheral neuropathy), and mental and behavioral changes. The disorder usually develops late in life and worsens over ...
    https://medlineplus.gov/genetics/gene/fmr1 - Genetics
  3. RELN gene 
    ... DF, Mondimore FM, Schweizer B; National Institute of Mental Health Genetics Initiative Bipolar Disorder Consortium; DePaulo JR Jr, Gershon ES, McMahon FJ, ...
    https://medlineplus.gov/genetics/gene/reln - Genetics
  4. POLG gene 
    ... Huttenlocher syndrome is characterized by seizures, loss of mental and movement abilities (psychomotor regression), and liver disease. The liver disease in Alpers-Huttenlocher syndrome can ...
    https://medlineplus.gov/genetics/gene/polg - Genetics
  5. TPP1 gene 
    ... cause CLN2 disease. This condition impairs motor and mental development, typically starting in early childhood, causing gradually worsening movement disorders and a decline in intellectual function. In addition, ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  6. CLN5 gene 
    ... CLN5 gene have been found to cause CLN5 disease. This condition impairs mental and motor development causing difficulty with walking and intellectual function. In addition, affected children often develop ... and symptoms of CLN5 disease typically appear around age 5 but can begin ...
    https://medlineplus.gov/genetics/gene/cln5 - Genetics
  7. PPT1 gene 
    ... PPT1 gene have been found to cause CLN1 disease. This condition impairs mental and motor development causing difficulty with walking, speaking, and intellectual function. In addition, affected children often develop ... and symptoms of CLN1 disease typically appear by age 18 months but can ...
    https://medlineplus.gov/genetics/gene/ppt1 - Genetics
  8. CLN6 gene 
    ... CLN6 gene have been found to cause CLN6 disease. This condition impairs motor and mental development, typically starting in early to late childhood, causing gradually worsening problems with movement and a decline in ... and symptoms of CLN6 disease do not appear until adulthood.Most CLN6 gene ...
    https://medlineplus.gov/genetics/gene/cln6 - Genetics
  9. ATN1 gene 
    ... Dentatorubral-pallidoluysian atrophy (DRPLA) is a progressive brain disorder that causes involuntary movements, mental and emotional problems, and a decline in thinking ...
    https://medlineplus.gov/genetics/gene/atn1 - Genetics
  10. MFSD8 gene 
    ... coordinating movements (ataxia), speech impairment, and vision loss. Mental functioning and motor skills (such as sitting and walking) decline with age. Individuals with CLN7 disease typically do not survive past their teens.MFSD8 ...
    https://medlineplus.gov/genetics/gene/mfsd8 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · next