Forms
The forms listed below are provided for physician use to allow ARUP to perform testing and/or interpret patient results.
Patient History Forms
- Alport Syndrome
- Angelman Syndrome
- Biochemical Genetic Testing
- Biotinidase Deficiency
- Connexin (Hearing Loss)
- Cystic Fibrosis (CF)
- Cytogenetic (Chromosome) Testing
- Ehlers-Danlos Syndrome Kyphoscoliotic (Type VI)
- Familial Adenomatous Polyposis
- Familial Cerebral Cavernous Malformation (CCM)
- Familial Mediterranian Fever (FMF)
- Family Specific Mutation Testing
- Fetal Fibronectin Testing
- Fetal Molecular Testing
- FG Syndrome
- Freeman-Sheldon Syndrome
- Galactosemia
- Genomic Microarray Testing
- Hearing Loss
- Hemoglobinopathy/Thalassemia
- Hemophilia A or B Gene
- Hereditary Hemorrhagic Telangiesctasia (HHT)
- Hypertrophic Cardiomyopathy (HCM)
- Juvenile Polyposis Syndrome (JPS)/Hereditary Hemorrhagic Telangiectasia (HHT)
- Laminopathies (LMNA) Gene
- Legius Syndrome
- Loeys-Dietz
- Lynch Syndrome/HNPCC
- Marfan Syndrome (FBN1) Gene
- Maternal Serum (Prenatal Screening for Down Syndrome) Testing
- Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency
- Molecular Genetic Testing
- Mucopolysaccharidosis (MPS)
- Multiple Endocrine Neoplasia 1 (MEN1) Gene
- Multiple Endocrine Neoplasia 2, RET Gene
- Noonan or Leopard Syndrome
- Ornithine Transcarbamylase Deficiency (OTC)
- Pancreatitis
- Prenatal Cytogenetics Testing
- Primary Carnitine Deficiency (SLC22A5)
- Primary Congenital Glaucoma (CYP1B1)
- PTEN Hamartoma Tumor Syndrome (PHTS)
- Pulmonary Arterial Hypertension (PAH)
- RASA-1-Related Disorders
- Rett Syndrome (MECP2) or CDKL5-Related Disorders
- Very Long Chain ACYL-CoA Dehydrogenase (VLCAD) Deficiency
- Von Hippel-Lindau Syndrome/Congenital Polycythemia (VHL)
- von Willebrand Disease (VWD)
- X-Chromosome Microarray Testing
Consent Forms
- Biochemical Genetic Testing
- Cytogenetic Testing
- deCODE ProstateCancer™ Test
- Hereditary Hemorrhagic Telangiectasia Deletion/Duplication
- Hereditary Hemorrhagic Telangiectasia Family Specific Mutation
- Hereditary Hemorrhagic Telangiectasia Full Gene Analysis
- Huntington Disease (required for Huntington Disease testing)
- Molecular Genetic Testing
