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 - 5 of 5 for Autosomal dominant Opitz "G/BBB" syndrome
  1. 22q11.2 deletion syndrome 
    ... members may be affected as well. 22q11.2DS Autosomal dominant Opitz G/BBB syndrome CATCH22 Cayler cardiofacial syndrome Conotruncal anomaly face syndrome ( ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  2. Opitz G/BBB syndrome 
    ... syndrome, X-linked Opitz G/BBB syndrome and autosomal dominant Opitz G/BBB syndrome. The two forms are distinguished by their genetic ... that this condition is underdiagnosed.The incidence of autosomal dominant Opitz G/BBB syndrome is unknown. It is part of a larger ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
  3. Learning about Velocardiofacial Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Congenital Heart Defects/Specifics ... Congenital Heart Defects ... Parathyroid Disorders/Genetics ... Parathyroid Disorders ... Cleft Lip and Palate/Specifics ... Cleft Lip and ...
    https://www.genome.gov/Genetic-Disorders/Velocardiofacial-Syndrome - External Health Links
  4. SPECC1L gene 
    ... 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome. J Med Genet. 2015 Feb;52(2):104- ...
    https://medlineplus.gov/genetics/gene/specc1l - Genetics
  5. Chromosome 22 
    ... Canning D, Zavod W, Quinn N, Rome J. Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion. Am J ...
    https://medlineplus.gov/genetics/chromosome/22 - Genetics