Previous GeneCards Identifiers for OGS2 Gene
This disorder, variously named the G, Opitz-G, or BBB syndrome, includes hypertelorism or telecanthus; laryngotracheoesophageal cleft; clefts of lip, palate, and uvula; swallowing difficulty and hoarse cry; genitourinary defects, especially hypospadias in males and splayed labia majora in females; mental retardation; and congenital heart defects.[supplied by OMIM, Jul 2002]
GeneCards Summary for OGS2 Gene
OGS2 (Opitz G Syndrome, Type II) is a Genetic Locus. Diseases associated with OGS2 include opitz gbbb syndrome, type ii.