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Results 1 - 10 of 116 for Developmental disorder
  1. HDAC8 gene 
    ... in people with Cornelia de Lange syndrome, a developmental disorder that affects many parts of the body. Researchers ... of HDAC8 PubMed HISTONE DEACETYLASE 8; HDAC8 INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WILSON-TURNER TYPE; WTS NCBI ...
    https://medlineplus.gov/genetics/gene/hdac8 - Genetics
  2. PPM1D gene 
    ... gene can cause Jansen-de Vries syndrome, a developmental disorder that affects many parts of the body. The ... Monaghan KG, de Vries P, Veltman JA; Deciphering Developmental Disorders Study; Lord CJ, Vissers LE, de Vries BB. ...
    https://medlineplus.gov/genetics/gene/ppm1d - Genetics
  3. ARX gene 
    ... CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29; XLID29 DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  4. FMR1 gene 
    ... 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. SMC1A gene 
    ... in people with Cornelia de Lange syndrome, a developmental disorder that affects many parts of the body. Researchers ... altered gene regulation probably underlies many of the developmental ... of the disorder, SMC1A gene variants often cause less significant delays ...
    https://medlineplus.gov/genetics/gene/smc1a - Genetics
  6. RAD21 gene 
    ... in people with Cornelia de Lange syndrome, a developmental disorder that affects many parts of the body. Variants ... altered gene regulation probably underlies many of the developmental problems ... of the disorder, RAD21 gene variants cause less significant delays in ...
    https://medlineplus.gov/genetics/gene/rad21 - Genetics
  7. SMC3 gene 
    ... found to cause Cornelia de Lange syndrome, a developmental disorder that affects many parts of the body. Researchers ... altered gene regulation probably underlies many of the developmental problems ... of the disorder, SMC3 gene variants often cause less significant delays ...
    https://medlineplus.gov/genetics/gene/smc3 - Genetics
  8. MIR17HG gene 
    ... MIR17HG gene cause Feingold syndrome type 2. This developmental disorder is characterized by abnormalities of the fingers and ... of the MIR17HG gene have been associated with developmental problems in a small ... disorder, which is characterized by impaired communication and social ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  9. GTF2I gene 
    ... in people with Williams syndrome, which is a developmental disorder characterized by mild to moderate intellectual disability or ...
    https://medlineplus.gov/genetics/gene/gtf2i - Genetics
  10. MECP2 gene 
    ... AUTISM METHYL-CpG-BINDING PROTEIN 2; MECP2 INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13; MRXS13 NCBI Gene ClinVar ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
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