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Results 1 - 10 of 24 for Intellectual developmental disorder 62
  1. DLG4-related synaptopathy 
    ... no history of the disorder in their family. Intellectual developmental disorder 62 intellectual developmental disorder, autosomal dominant 62 SHINE syndrome ...
    https://medlineplus.gov/genetics/condition/dlg4-related-synaptopathy - Genetics
  2. Guanidinoacetate methyltransferase deficiency 
    ... CD. Cerebral creatine deficiencies: a group of treatable intellectual ... Mol Genet Metab. 2013 Nov;110(3):255-62. doi: 10.1016/j.ymgme.2013.08.020. ...
    https://medlineplus.gov/...idinoacetate-methyltransferase-deficiency - Genetics
  3. Jansen-de Vries syndrome 
    ... history of the disorder in their family. IDDGIP Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold JDVS ... Novel truncating PPM1D mutation in a patient with intellectual disability. Eur J Med Genet. 2019 Jan;62(1):70-72. doi: 10.1016/j.ejmg. ...
    https://medlineplus.gov/genetics/condition/jansen-de-vries-syndrome - Genetics
  4. FMR1 gene 
    ... have learning disabilities, attention-deficit/hyperactivity disorder (ADHD), intellectual disability, or developmental disorders that affect communication and social interaction (such as ...
    https://medlineplus.gov/genetics/gene/fmr1 - Genetics
  5. PPP2R5D-related intellectual disability 
    PPP2R5D-related intellectual disability is a neurological disorder characterized by moderate to severe developmental delay and intellectual disability. Affected individuals have weak muscle tone (hypotonia); delayed development of motor skills, such as ...
    https://medlineplus.gov/.../ppp2r5d-related-intellectual-disability - Genetics
  6. Aromatic l-amino acid decarboxylase deficiency 
    ... the eyes. Additional signs and symptoms typically include developmental delays and intellectual disabilities. Movement disorders are common in people with AADC deficiency. Involuntary ...
    https://medlineplus.gov/...tic-l-amino-acid-decarboxylase-deficiency - Genetics
  7. Chromosome 1 
    ... Some people with a 1q21.1 microduplication have developmental delays, intellectual disabilities, or features of autism spectrum disorder, which ischaracterized by impaired communication and socialization skills. ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  8. Smith-Lemli-Opitz syndrome 
    Smith-Lemli-Opitz syndrome is a developmental ... features of autism, a developmental condition that affects communication ...
    https://medlineplus.gov/.../condition/smith-lemli-opitz-syndrome - Genetics
  9. STAMBP gene 
    ... people with microcephaly-capillary malformation syndrome, an inherited disorder characterized by an abnormally small head size (microcephaly), profound developmental delay and intellectual disability, recurrent seizures (epilepsy), and abnormalities of small ...
    https://medlineplus.gov/genetics/gene/stambp - Genetics
  10. 10q26 deletion syndrome 
    ... change are distinctive facial features, mild to moderate intellectual ... disorder (ADHD), poor impulse control (impulsivity), or exhibit autistic ...
    https://medlineplus.gov/genetics/condition/10q26-deletion-syndrome - Genetics
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