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Results 31 - 40 of 126 for Intellectual "disability," autosomal dominant 3
  1. Megalencephalic leukoencephalopathy with subcortical cysts 
    ... this condition typically have only mild to moderate intellectual disability.There are three types of megalencephalic leukoencephalopathy with subcortical cysts, which ...
    https://medlineplus.gov/...eukoencephalopathy-with-subcortical-cysts - Genetics
  2. 3q29 microdeletion syndrome 
    ... can influence the features of this condition. chromosome 3 This condition has an autosomal dominant pattern of inheritance, which means the deletion occurs ...
    https://medlineplus.gov/.../condition/3q29-microdeletion-syndrome - Genetics
  3. 3q29 microduplication syndrome 
    ... can influence the features of this condition. chromosome 3 This condition has an autosomal dominant pattern of inheritance, which means the duplication occurs ...
    https://medlineplus.gov/.../condition/3q29-microduplication-syndrome - Genetics
  4. Frontonasal dysplasia 
    ... halves of the brain (the corpus callosum), and intellectual disability.There are at least three types of frontonasal dysplasia that are distinguished by ...
    https://medlineplus.gov/genetics/condition/frontonasal-dysplasia - Genetics
  5. Chromosome 22 
    ... for many of the characteristic features of 22q13.3 deletion syndrome, such as developmental delay, intellectual disability, and absent or severely delayed speech. Additional genes ...
    https://medlineplus.gov/genetics/chromosome/22 - Genetics
  6. 22q13.3 deletion syndrome 
    ... the chromosome deletion to their children.When 22q13.3 deletion syndrome is inherited, its inheritance pattern is considered autosomal dominant because a deletion in one copy of chromosome ...
    https://medlineplus.gov/genetics/condition/22q133-deletion-syndrome - Genetics
  7. MSX1 gene 
    ... Lin BP, Hu JC. Novel MSX1 frameshift causes autosomal-dominant oligodontia. J Dent Res. 2006 Mar;85(3):267-71. doi: 10.1177/154405910608500312. Citation on ...
    https://medlineplus.gov/genetics/gene/msx1 - Genetics
  8. Alzheimer's disease 
    ... Alzheimer disease 2 Genetic Testing Registry: Alzheimer disease 3 Genetic Testing Registry: Alzheimer disease 4 Alzheimer disease 2 Early-onset autosomal dominant Alzheimer disease National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/alzheimers-disease - Genetics
  9. Pitt-Hopkins syndrome 
    ... Citation on PubMed Sweatt JD. Pitt-Hopkins Syndrome: intellectual disability due to loss of TCF4-regulated gene transcription. Exp Mol Med. 2013 May 3;45(5):e21. doi: 10.1038/emm.2013. ...
    https://medlineplus.gov/genetics/condition/pitt-hopkins-syndrome - Genetics
  10. Cantú syndrome 
    ... delayed speech, and some affected children have mild intellectual disability or learning problems. Cantú syndrome is a rare condition. About three dozen affected individuals have been reported in the ...
    https://medlineplus.gov/genetics/condition/cantu-syndrome - Genetics
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