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 149 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. PROKR2 gene 
    ... article on PubMed Central Sarfati J, Dode C, Young J. Kallmann syndrome caused by mutations in the PROK2 and PROKR2 ...
    https://medlineplus.gov/genetics/gene/prokr2 - Genetics
  3. 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
  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. RPS6KA3 gene 
    ... 2003.06.001. Citation on PubMed Hanauer A, Young ID. Coffin-Lowry syndrome: clinical and molecular features. J Med Genet. 2002 ...
    https://medlineplus.gov/genetics/gene/rps6ka3 - Genetics
  8. 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
  9. PROK2 gene 
    ... 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/gene/prok2 - Genetics
  10. HNF1B gene 
    ... a type of maturity-onset diabetes of the young (MODY) called renal cysts and diabetes (RCAD) syndrome (described above). Other features of 17q12 deletion syndrome ...
    https://medlineplus.gov/genetics/gene/hnf1b - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next