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 10 for Intellectual "disability," "X-linked" 20
  1. PHF8 gene 
    ... the PHF8 gene have been found to cause X-linked intellectual disability, Siderius type. This condition is characterized by mild ... cleft lip and palate found in males with X-linked intellectual disability, Siderius type. More About This Health Condition histone ...
    https://medlineplus.gov/genetics/gene/phf8 - Genetics
  2. ARX gene 
    ... the X chromosome, this condition is known as X-linked intellectual disability (XLID) or sometimes nonsyndromic XLID. XLID can occur ... screening of ARX gene in Iranian families with X-linked intellectual disability. Arch Iran Med. 2012 Jun;15(6):361- ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  3. HCFC1 gene 
    ... gene have also been found in individuals with X-linked intellectual disability. These individuals have delayed development and other neurological ... A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual ... Epub 2012 Sep 20. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/hcfc1 - Genetics
  4. HSD17B10 gene 
    ... in the HSD17B10 gene causes a form of X-linked intellectual disability called MRXS10. This disorder is characterized by intellectual ...
    https://medlineplus.gov/genetics/gene/hsd17b10 - Genetics
  5. AFF2 gene 
    ... proteins: insights into the molecular pathology of FRAXE intellectual disability. Hum Mol Genet. 2011 May 15;20(10):1873-85. doi: 10.1093/hmg/ddr069. ...
    https://medlineplus.gov/genetics/gene/aff2 - Genetics
  6. PQBP1 gene 
    ... Wanker EE, Kalscheuer VM. The X-chromosome-linked intellectual disability protein PQBP1 is a component of neuronal RNA granules and regulates the appearance of stress granules. Hum Mol Genet. 2011 Dec 15;20(24):4916-31. doi: 10.1093/hmg/ddr430. ...
    https://medlineplus.gov/genetics/gene/pqbp1 - Genetics
  7. CACNA1F gene 
    ... mutation has also been found to cause an X-linked retinal disorder in a large ... disability. The CACNA1F mutation associated with this condition alters ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  8. MED12 gene 
    ... to cause FG syndrome, which is characterized by intellectual disability, behavioral problems, and physical abnormalities including weak muscle ... is unclear how the genetic changes lead to intellectual disability and the other features of FG syndrome. More ...
    https://medlineplus.gov/genetics/gene/med12 - Genetics
  9. L1CAM gene 
    ... People with L1 syndrome often have brain abnormalities, intellectual disability, and movement problems. The L1CAM gene mutations that ... Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus ... 2016 May 20. Citation on PubMed Finckh U, Schroder J, Ressler ...
    https://medlineplus.gov/genetics/gene/l1cam - Genetics
  10. SLC16A2 gene 
    ... the brain disrupts normal brain development, resulting in intellectual disability and problems with movement.If T3 is not ... Su H, Molinero MR, Rogers RC, Schwartz CE. X-linked MCT8 gene mutations: ... 2005 Oct;20(10):852-7. doi: 10.1177/08830738050200101601. Citation ...
    https://medlineplus.gov/genetics/gene/slc16a2 - Genetics