Opitz G/BBB Syndrome, Autosomal Dominant

Synonym(s): Hypertelorism with Esophageal Abnormality and Hypospadias


OMIMRelated Disorders

Test Type
Molecular (3)
Multi-Gene Panel (1)
Test Method
Del/Dup (CNV) (1)
Sequencing, Capillary (Sanger) (1)
Sequencing, Next Gen (1)
Prenatal (1)
Carrier (1)
Lab Location

Opitz G/BBB Syndrome, Sequencing MID1 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 8-9 weeks
price: contact lab
Abnormal/Ambiguous Genitalia Sequencing Test
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 3-4 weeks
price: contact lab
22q11.2 Deletion/Duplication Analysis
method(s): ◦ Del/Dup (CNV) 
Children's Hospital of Los Angeles, Center for Personalized Medicine Laboratory - Los Angeles, CA, USA