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Results 61 - 70 of 95 for Intellectual "disability," autosomal recessive 11
  1. ... these individuals. Some people with this condition have intellectual disability or developmental delay, but others have normal intelligence. ... disorders. SLC25A15 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  2. ... for too long, they can cause coma and intellectual disability.The signs and symptoms of lysinuric protein intolerance ... unclear. SLC7A7 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  3. ... disrupts brain development. Most affected children have severe intellectual disability and do not develop skills such as reaching ... unknown. ST3GAL5 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  4. ... ganglia, which are regions that help control movement. Intellectual disability may also occur.The severity of glutaric acidemia ... I. GCDH This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  5. ... area of the brain called the basal ganglia. Intellectual disability has been reported in some affected individuals.The ... cells. PSMB8 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  6. ... tissues of the body. Affected individuals may have intellectual disability, distinctive facial features, and skeletal abnormalities. Characteristic facial ...
  7. ... the roof of the mouth (cleft palate), or intellectual disability. The prevalence of ophthalmo-acromelic syndrome is not ... unknown. SMOC1 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  8. ... Affected individuals may have developmental delay and progressive intellectual disability, although intelligence is unaffected in some people with ... cells. GUSB This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  9. ... common features of 3MC syndrome include developmental delay, intellectual disability, hearing loss, and slow growth after birth resulting ... COLEC11 MASP1 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  10. ... muscle tone (hypotonia), seizures, speech difficulties, developmental delay, intellectual disability, and autistic behaviors that affect communication and social ...
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