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Results 11 - 20 of 65 for Dysmorphism
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  1. 17q12 deletion syndrome is a condition that results from the deletion of a small piece of chromosome 17 in each cell. The deletion occurs on the long (q) arm ...
  2. ... L, Chamova T. CTDP1-Related Congenital Cataracts, Facial Dysmorphism, and Neuropathy. 2010 Mar 2 [updated 2022 Oct ... Citation on PubMed Kalaydjieva L. Congenital cataracts-facial dysmorphism-neuropathy. Orphanet J Rare Dis. 2006 Aug 29; ...
  3. Birth Defects (National Library of Medicine)  
    What are birth defects? A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the ...
  4. ... AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome Autosomal dominant intellectual disability 25 XGS Genetic ... AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome AHDC1-related intellectual disability-obstructive sleep apnea- ...
  5. ... Autosomal dominant intellectual disability-17 Intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome PACS1-related syndrome Schuurs-Hoeijmakers syndrome ...
  6. Esophageal Atresia and Tracheoesophageal Fistula (American Academy of Family Physicians)  
    Birth Defects/Specifics ... Birth Defects ... Esophagus Disorders/Children ... Esophagus Disorders ... Fistulas/Children ... Fistulas ... Tracheal Disorders/Children ... Tracheal Disorders
  7. Psychedelic and Dissociative Drugs From the National Institutes of Health (National Institute on Drug Abuse)  
    Club Drugs/Start Here ... Club Drugs ... Drug Use and Addiction/Specifics ... Drug Use and Addiction ... National Institute on Drug Abuse ... From the National Institutes of Health
  8. Peripheral Nerve Disorders (National Library of Medicine)  
    What are peripheral nerves? Nerves are like wires that carry messages back and forth between your brain and your body. Your peripheral nerves branch off ...
  9. ... rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. J Med Genet. ...
  10. ... syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its ...
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