XomeDxSlice Tool

Now Available - NEW XomeDxSlice Xpanded – Custom slice testing with trio analysis for lists >150 genes.



If cutting and pasting from another document, please be sure to list EITHER one gene symbol per line OR enter a comma-separated list.



You may also use this search to review average exome sequencing coverage by entering the gene symbol below.


What do you want to do?

Place an e-order of this Slice on a specific patient through the GeneDx Portal  
Obtain a Slice ID to order testing with a printed requisition form  
Only email the gene list to myself and/or others at this time  

Enlarged tonsils

Select all: Gene symbolChrAvg % covered at 10xLocus TypeNoteOMIMPrevious symbol(s)Phenotype(s)Slice(s)
AKT219q13.2100%gene with protein product164731Abnormal circulating insulin level; Acanthosis nigricans; Autosomal dominant inheritance; Autosomal recessive inheritance; Decreased adiponectin level; Decreased serum leptin; Enlarged tonsils; Gynecomastia; Hemihypertrophy; Hepatic steatosis; Hepatomegaly; Hypertriglyceridemia; Hypoglycemic coma; Hypoglycemic seizures; Hypoketotic hypoglycemia; Increased hepatic glycogen content; Increased intraabdominal fat; Insulin resistance; Insulin-resistant diabetes mellitus; Large for gestational age; Late onset; Lipodystrophy; Neonatal hypoglycemia; Nonketotic hypoglycemia; Oligomenorrhea; Polycystic ovaries; Seizures; Truncal obesity; Type II diabetes mellitus
CD40LGXq26.399.75%gene with protein product300386HIGM1, IMD3, TNFSF5Absence of lymph node germinal center; Chronic hepatitis; Decreased T cell activation; Diarrhea; Dysgammaglobulinemia; Enlarged tonsils; Gingivitis; Hemolytic anemia; Hepatitis; Hepatomegaly; IgA deficiency; IgE deficiency; IgG deficiency; Immunodeficiency; Impaired Ig class switch recombination; Impaired memory B cell generation; Increased IgM level; Neutropenia; Recurrent bacterial infections; Splenomegaly; Stomatitis; Thrombocytopenia; X-linked recessive inheritanceAutoimmune Disorders ; Common Variable Immune Deficiency ; Inflammatory Bowel Disease ; Primary Immunodeficiency
IDUA4p16.3100%gene with protein product252800Abnormal CNS myelination; Abnormal diaphysis morphology; Abnormal heart valve morphology; Abnormal nerve conduction velocity; Abnormal pyramidal signs; Abnormal vertebral morphology; Abnormality of epiphysis morphology; Abnormality of the clavicle; Abnormality of the elbow; Abnormality of the ribs; Abnormality of the tonsils; Anteverted nares; Aortic regurgitation; Aortic valve stenosis; Autosomal recessive inheritance; Biconcave vertebral bodies; Broad face; Broad nasal tip; Calvarial hyperostosis; Camptodactyly of finger; Cardiomyopathy; Cerebral palsy; Chronic diarrhea; Coarse facial features; Constrictive median neuropathy; Corneal opacity; Coxa valga; Death in infancy; Depressed nasal bridge; Depressivity; Diaphyseal thickening; Dolichocephaly; Dysostosis multiplex; Enlarged tonsils; Everted lower lip vermilion; Feeding difficulties; Flared iliac wings; Flexion contracture; Frontal bossing; Full cheeks; Generalized hirsutism; Genu valgum; Gingival overgrowth; Glaucoma; Global developmental delay; Hearing impairment; Hepatomegaly; Hepatosplenomegaly; Hernia; Hirsutism; Hydrocephalus; Hypertension; Hypoplasia of the femoral head; Hypoplasia of the odontoid process; Inguinal hernia; Intellectual disability; J-shaped sella turcica; Joint stiffness; Kyphosis; Large face; Limitation of joint mobility; Macrocephaly; Macroglossia; Mandibular prognathia; Microdontia; Micrognathia; Mitral regurgitation; Mucopolysacchariduria; Muscular hypotonia; Narrow pelvis bone; Neurodegeneration; Obstructive sleep apnea; Opacification of the corneal stroma; Pes cavus; Progressive neurologic deterioration; Pulmonary arterial hypertension; Recurrent ear infections; Recurrent respiratory infections; Retinopathy; Rhinitis; Scoliosis; Sensorineural hearing impairment; Short clavicles; Short neck; Short stature; Skeletal dysplasia; Sleep disturbance; Spinal canal stenosis; Splenomegaly; Thick eyebrow; Thick vermilion border; Tracheal stenosis; Umbilical hernia; Urinary glycosaminoglycan excretion; Wide nasal bridge; Wide nose

The gene coverage data provided by GeneDx represent an estimate based on previous results, but the specific sequencing coverage data for the genes selected may vary from individual to individual, and cannot be predicted exactly. Changes to an approved gene list can only be made by contacting GeneDx directly at 888-729-1206 and asking to speak with a member of our Whole Exome Sequencing Laboratory.


Customize below OR enter Suggested Slice ID on printed requisition form
(e.g. 706 XomeDxSlice - Slice ID: CS-Albinism).

Suggested Slice IDSuggested Gene List Name
CS-AAAplastic Anemia
CS-AutoImmuneAutoimmune Disorders
CS-BBSBardet-Biedl Syndrome
CS-BMFBone Marrow Failure Syndromes
CS-CVIDCommon Variable Immune Deficiency
CS-CKUTCongenital Kidney and Urinary Tract (CKUT) Anomalies
CS-DSDDisorders of Sex Development
CS-EDEctodermal Dysplasia
CS-FAFanconi Anemia
CS-AnemiaHemolytic Anemia
CS-IBDInflammatory Bowel Disease
CS-MaleInfMale Infertility
CS-WWSMuscular dystropy-dystroglycanopathy (Walker-Warburg)
CS-NephroticNephrotic Syndrome
CS-PPKCIPalmoplantar keratoderma plus congenital ichthyosis
CS-Primary ImmunodefPrimary Immunodeficiency
CS-SRTDShort-Rib Thoracic Dysplasia
CS-WSWaardenburg Syndrome