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Results 1 - 5 of 5 for Intellectual "disability," autosomal dominant 13
  1. CACNA1A gene 
    ... genes in each cell. Features associated with 19p13.13 deletion syndrome include an unusually large head size (macrocephaly), tall stature, intellectual disability, seizures, ataxia, and other health problems. Researchers are ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  2. WASHC5 gene 
    ... B, Leppert M, Fink JK. Novel locus for autosomal dominant hereditary spastic ... Spastic Paraplegia 8. 2008 Aug 13 [updated 2020 May 21]. In: Adam MP, Feldman ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  3. ELN gene 
    ... and vascular disease. Trends Cardiovasc Med. 2003 Jul;13(5):176-81. doi: ... of autosomal-dominant cutis laxa with report of five ELN mutations. ...
    https://medlineplus.gov/genetics/gene/eln - Genetics
  4. TBC1D24 gene 
    ... short fingers and toes (osteodystrophy); developmental delay and intellectual disability (previously called mental retardation); and seizures. Some people ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  5. MSX1 gene 
    ... a characteristic facial appearance, delayed growth and development, intellectual disability, and seizures. A loss of the MSX1 gene ... Lin BP, Hu JC. Novel MSX1 frameshift causes autosomal-dominant oligodontia. J Dent Res. 2006 Mar;85(3): ...
    https://medlineplus.gov/genetics/gene/msx1 - Genetics