Specific code 2015 ICD-9-CM Diagnosis Code 279.11
Digeorge's syndrome
  • 2015
  • Billable Code
  • ICD-9-CM 279.11 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 279.11 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
Disease Synonyms
  • Chromosome 22q11.2 deletion
  • DiGeorge sequence
  • Digeorge syndrome
  • Digeorges syndrome
Clinical Information
  • A congenital anomaly characterized by immunodeficiency, abnormal facies, congenital heart disease, hypocalcemia, and increased susceptibility to infections. Pathologic characteristics include conotruncal abnormalities and absence or hypoplasia of thymus and parathyroid glands. Digeorge syndrome is associated with abnormalities of chromosome 22. Also known as digeorge anomaly
  • A developmental defect of derivatives of the third and fourth pharyngeal pouches, almost always associated with agenesis or hypoplasia of the thymus and parathyroid gland, characteristic facies with downslanting palpebral fissures and ocular and nasal anomalies, hypocalcemia, cardiovascular anomalies, immunodeficiency, and other variable abnormalities. Patients who survive infancy are usually mentally retarded. Digeorge syndrome is considered by some researchers as a developmental field defect consisting of several casually distinct disorders, rather than a distinct syndromic entity. Conditions associated with the development of digeorge syndrome include diabetic embryopathy, fetal alcohol syndrome, and zellweger syndrome. Major features of this syndrome have been designated by the newcastle upon tyne group catch 22 (cardiac, abnormal facies, thymic hypoplasia, cleft palate, and hypocalcemia), the number 22 indicating deletion of the long arm of chromosome 22 (22q11)
  • Branchial arch defects with craniofacial abnormalities, hearing loss, short stature, and learning difficulty
  • Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the thymus and parathyroid glands resulting in t-cell immunodeficiency, hypocalcemia, defects in the outflow tract of the heart, and craniofacial anomalies
  • Congenital syndrome with the absence of the thymus and parathyroids causing impairment of cellular immunity; immunoglobulin levels are normal
Applies To
  • Pharyngeal pouch syndrome
  • Thymic hypoplasia
Convert to ICD-10-CM: 279.11 converts directly to:
  • 2015 ICD-10-CM D82.1 Di George's syndrome
ICD-9-CM Volume 2 Index entries containing back-references to 279.11:
  • Di George's syndrome (thymic hypoplasia) 279.11
  • Hypoplasia, hypoplasis 759.89
    • thymus (gland) 279.11
  • Pharyngeal - see also condition
    • pouch syndrome 279.11
  • Syndrome - see also Disease
    • DiGeorge's (thymic hypoplasia) 279.11
    • pharyngeal pouch 279.11
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 279.11 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2015 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.