D82.1
BillableDi George's syndrome
Di George's syndrome
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Pharyngeal pouch syndrome
- Thymic alymphoplasia
- Thymic aplasia or hypoplasia with immunodeficiency
Includes
Conditions included under this code
- defects in the complement system
- immunodeficiency disorders, except human immunodeficiency virus [HIV] disease
- sarcoidosis
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(6)
D82.0Wiskott-Aldrich syndrome
D82.2Immunodeficiency with short-limbed stature
D82.3Immunodef fol heredit defctv response to Epstein-Barr virus
D82.4Hyperimmunoglobulin E [IgE] syndrome
D82.8Immunodeficiency associated with oth major defects
D82.9Immunodeficiency associated with major defect, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(80)
SNOMED CT
UMLS
- 22q deletion syndromeC0012236
- 22q- syndromeC0012236
- 22q11.2 Deletion SyndromeC0012236
- CATCH 22C0012236
- CATCH22C0012236
- CHROMOSOME 22q11.2 DELETION SYNDROMEC0012236
- Catch22C0012236
- DGSC0012236
- DIGEORGE SYNDROMEC0012236
- Di George's syndromeC0012236
- DiGeorge AnomalyC0012236
- DiGeorge SequenceC0012236
- DiGeorge SyndromeC0012236
- DiGeorge sequenceC0012236
- DiGeorge syndromeC0012236
- DiGeorge's SyndromeC0012236
- DiGeorge's syndromeC0012236
- Familial Third and Fourth Pharyngeal Pouch SyndromeC0012236
- HYPOPLASIA OF THYMUS AND PARATHYROIDSC0012236
- Hypoplasia of Thymus and ParathyroidsC0012236
- Pharyngeal Pouch SyndromeC0012236
- Pharyngeal pouch syndromeC0012236
- Syndrome, DiGeorgeC0012236
- THIRD AND FOURTH PHARYNGEAL POUCH SYNDROMEC0012236
- Third and Fourth Pharyngeal Pouch SyndromeC0012236
- Thymic Aplasia SyndromeC0012236
- Thymic-parathyroid aplasiaC0012236
- di george syndromeC0012236
- di george's syndromeC0012236
- di georges syndromeC0012236
- digeorge anomalyC0012236
- digeorge sequenceC0012236
- digeorge syndromeC0012236
- digeorge syndromesC0012236
- digeorge's syndromeC0012236
- digeorges syndromeC0012236
- pharyngeal pouch syndromeC0012236
- syndrome di georgeC0012236
- thymic aplasia syndromeC0012236
- thymic hypoplasiaC0012236
- Thymic alymphoplasiaC0543687
- Thymic aplasia or hypoplasia with immunodeficiencyC2873847
Clinical Terms
- Third and Fourth Pharyngeal Pouch Syndrome
- digeorge's syndrome
- digeorge syndromes
- DGS
- digeorge anomaly
- Pharyngeal Pouch Syndrome
- DIGEORGE SYNDROME
- Thymic Aplasia Syndrome
- DiGeorge Sequence
- 22q11.2 Deletion Syndrome
- digeorges syndrome
- CATCH 22
- Thymic alymphoplasia
- Familial Third and Fourth Pharyngeal Pouch Syndrome
- 22q- syndrome
- CATCH22
- Congenital thymic aplasia
- CHROMOSOME 22q11.2 DELETION SYNDROME
- Syndrome, DiGeorge
- di george syndrome
- Congenital absence of thymus
- di georges syndrome
- 22q deletion syndrome
- Aplasia of thymus gland with immunodeficiency
- Aplasia of thymus
- HYPOPLASIA OF THYMUS AND PARATHYROIDS
- thymic hypoplasia
- Dysplasia of thymus gland with immunodeficiency
- syndrome di george
- Thymic aplasia or dysplasia with immunodeficiency
- Thymic aplasia or hypoplasia with immunodeficiency
- Thymic-parathyroid aplasia
Frequently Asked Questions
What is the ICD-10 code for di george's syndrome?
The ICD-10-CM code for di george's syndrome is D82.1. The full clinical description is "Di George's syndrome". D82.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D82.1 mean?
ICD-10-CM code D82.1 represents “Di George's syndrome”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D82.1 a billable code?
Yes, D82.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D82.1 in?
D82.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D82.1?
D82.1 has Excludes1 notes indicating codes that cannot be used together with it, including: autoimmune disease (systemic) NOS (M35.9); functional disorders of polymorphonuclear neutrophils (D71); human immunodeficiency virus [HIV] disease (B20); and 1 more.
What SNOMED CT codes does D82.1 map to?
D82.1 maps to 5 SNOMED CT concepts: 702623002, 24181002, 91918005, 48119005, 190995003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D82.1?
D82.1 is linked to 3 UMLS Concept Unique Identifiers: C0012236, C0543687, C2873847. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D82.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like di george's syndrome affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D82.1?
D82.1 maps to the ICD-11 code: LD44.N0 (CATCH 22 phenotype).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.