Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 89 for Young syndrome
  1. Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant 
    ... variant Ohdo syndrome, SBBYS variant Say-Barber-Biesecker-Young-Simpson syndrome Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome SBBYS variant of Ohdo syndrome SBBYSS Young-Simpson syndrome Genetic Testing Registry: Blepharophimosis - intellectual disability syndrome, SBBYS ...
    https://medlineplus.gov/...ay-barber-biesecker-young-simpson-variant - Genetics
  2. Coffin-Lowry syndrome 
    ... gov COFFIN-LOWRY SYNDROME; CLS PubMed Hanauer A, Young ID. Coffin-Lowry syndrome: clinical and molecular features. J Med Genet. 2002 ...
    https://medlineplus.gov/genetics/condition/coffin-lowry-syndrome - Genetics
  3. Wiedemann-Rautenstrauch syndrome 
    ... do not survive past infancy, others live into young adulthood. Wiedemann-Rautenstrauch syndrome is a rare disorder. Its prevalence is unknown. ...
    https://medlineplus.gov/.../wiedemann-rautenstrauch-syndrome - Genetics
  4. Down syndrome 
    ... Lannigan E. Neurobehavioral disorders in children, adolescents, and young adults with Down syndrome. Am J Med Genet C Semin Med Genet. ...
    https://medlineplus.gov/genetics/condition/down-syndrome - Genetics
  5. FOXG1 syndrome 
    ... to sit or walk without assistance. Babies and young children with FOXG1 syndrome often have feeding problems, sleep disturbances, seizures, irritability, ...
    https://medlineplus.gov/genetics/condition/foxg1-syndrome - Genetics
  6. Williams syndrome 
    ... phobias are common among people with this disorder.Young children with Williams syndrome have distinctive facial features including a broad forehead, ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
  7. Kallmann syndrome 
    ... Toublanc JE, Wolczynski S, Delpech M, Petit C, Young J, Hardelin JP. Kallmann syndrome: mutations in the genes encoding prokineticin-2 and ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  8. Cardiofaciocutaneous syndrome 
    ... Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G. The cardiofaciocutaneous syndrome. J Med Genet. 2006 Nov;43(11):833- ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  9. Maturity-onset diabetes of the young 
    ... TYPE 1; MODY1 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 2; MODY2 RENAL CYSTS AND DIABETES SYNDROME; RCAD MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3; MODY3 MATURITY-ONSET DIABETES OF THE ...
    https://medlineplus.gov/.../maturity-onset-diabetes-of-the-young - Genetics
  10. SOX2 anophthalmia syndrome 
    ... Katowitz J, Schimmenti LA, Hummel M, Fitzpatrick DR, Young TL. Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters. Am ...
    https://medlineplus.gov/.../condition/sox2-anophthalmia-syndrome - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · next