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18 results
  1. ... cases. Learn more about the gene associated with Gorlin-Chaudhry-Moss syndrome SLC25A24 Inheritance In individuals with an SLC25A24 gene ...
  2. ... within cells. Health Conditions Related to Genetic Changes Gorlin-Chaudhry-Moss syndrome At least two mutations in the SLC25A24 gene have been found to cause Gorlin-Chaudhry-Moss syndrome. This condition, which has been found only in ...
  3. ... published></health-condition-summary><health-condition-summary ><name >Gorlin-Chaudhry-Moss syndrome</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
  4. ... SLC25A24 pathogenic variant and clinical findings suggestive of Gorlin-Chaudhry-Moss syndrome included in the report by Ehmke et al [ ... Additionally, earlier reports of individuals clinically diagnosed with Gorlin-Chaudhry-Moss syndrome and Petty syndrome included individuals in their 30s ...
  5. ... syndrome GCL, see Krabbe disease GCM syndrome, see Gorlin-Chaudhry-Moss syndrome GCMS, see Gorlin-Chaudhry-Moss syndrome GCPS, see Greig cephalopolysyndactyly syndrome GD, see Gaucher ...
  6. ... topic><topic ><url >https://medlineplus.gov/genetics/condition/gorlin-chaudhry-moss-syndrome</url><title >Gorlin-Chaudhry-Moss syndrome</title><other_ ...
  7. ... anomalies, patent ductus arteriosus, and normal intelligence, see Gorlin-Chaudhry-Moss syndrome Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of ...
  8. ... amaurosis , X-linked juvenile retinoschisis , Senior-Løken syndrome , Gorlin-Chaudhry-Moss syndrome , Down syndrome , and fragile X syndrome . Inheritance Farsightedness ...
  9. ... Frontonasal dysplasia: MedlinePlus Genetics (National Library of Medicine) Gorlin-Chaudhry-Moss syndrome: MedlinePlus Genetics (National Library of Medicine) Greig cephalopolysyndactyly ...
  10. NLM Digital Collections - Eponymous syndromes : MEDLARS indexing instructions 
    Publication: [Bethesda, Md..] : National Library of Medicine, Bibliographic Services Division, Index Section, 1970
    ... CYSTS (IM) JAW DISEASES (IM) AUTOSOME ABNORMALITIES (NIM) Gorlin-Chaudhry-Moss syndrome CRANIOFACIAL DYSOSTOSIS (IM) DUCTUS ARTERIOSIS, PATENT (IM) HYPERTRICHOSIS ( ...
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