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Results 1 - 10 of 10 for "X-linked" syndromic intellectual disability
  1. ... linked mental retardation Siderius type Genetic Testing Registry: Syndromic X-linked intellectual disability Siderius type X-linked intellectual disability, Siderius type ...
  2. ... syndrome Spermine synthase deficiency SRS Genetic Testing Registry: Syndromic X-linked intellectual disability Snyder type X-linked intellectual disability, Snyder type ...
  3. ... mental retardation syndrome Trisomy Xq28 Genetic Testing Registry: Syndromic X-linked intellectual disability Lubs type Proximal Xq28 duplication syndrome National Organization ...
  4. ... linked intellectual deficit, Najm type Genetic Testing Registry: Syndromic X-linked intellectual disability Najm type National Organization for Rare Disorders (NORD) ...
  5. ... their sons. MRXS13 PPMX X-linked mental retardation, syndromic 13 Genetic Testing Registry: Rett syndrome X-linked intellectual disability-psychosis-macroorchidism syndrome National Organization for Rare Disorders ( ...
  6. ... marfanoid features Genetic Testing Registry: X-linked intellectual disability with marfanoid habitus Lujan-Fryns syndrome National Organization for Rare Disorders (NORD) INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUJAN-FRYNS TYPE; MRXSLF PubMed Lerma-Carrillo I, ...
  7. ... mild learning disabilities. It is unclear if these disabilities are related to the gene mutation or occur by chance. ... PubMed Gilfillan GD, Selmer KK, ...
  8. ... which is a form of X-linked intellectual disability. However, researchers speculate that it may actually be part of the same disease spectrum as Cornelia de Lange ... NCBI Gene ClinVar Deardorff ...
  9. ... associated with some cases of moderate to severe X-linked intellectual disability without other features of the syndromes described above. ... AS AUTISM METHYL-CpG-BINDING PROTEIN 2; MECP2 INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13; MRXS13 NCBI Gene ClinVar Adkins NL, Georgel ...
  10. ... abnormalities (typically affecting the toes), hearing loss, and intellectual disabilities. OFCD syndrome is very rare; the incidence is ...