D80.0
BillableHereditary hypogammaglobulinemia
Hereditary hypogammaglobulinemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Autosomal recessive agammaglobulinemia (Swiss type)
- X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
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) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- Alveolar proteinosis10501004
- PAP - Pulmonary alveolar proteinosis10501004
- Pulmonary alveolar lipoproteinosis10501004
- Pulmonary alveolar proteinosis10501004
- Proteinosis59714007
- BTK-deficiency65880007
- Bruton tyrosine kinase deficiency65880007
- Bruton's agammaglobulinaemia65880007
- Bruton's agammaglobulinemia65880007
- Bruton's hypogammaglobulinaemia65880007
- Bruton's hypogammaglobulinemia65880007
- Bruton's type agammaglobulinaemia65880007
- Bruton's type agammaglobulinemia65880007
- X linked agammaglobulinaemia65880007
- X linked agammaglobulinemia65880007
- X-linked agammaglobulinaemia65880007
- X-linked agammaglobulinemia65880007
- XLA - X-linked agammaglobulinaemia65880007
- XLA - X-linked agammaglobulinemia65880007
- Congenital agammaglobulinaemia116133005
- Congenital agammaglobulinemia116133005
- Hypogammaglobulinaemia119250001
- Hypogammaglobulinemia119250001
- Fleisher syndrome234533006
- Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinaemia234533006
- Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia234533006
- X-linked agammaglobulinaemia with growth hormone deficiency234533006
- X-linked agammaglobulinemia with growth hormone deficiency234533006
- Autosomal agammaglobulinaemia with absent B-cells234534000
- Autosomal agammaglobulinemia with absent B-cells234534000
- Functional antibody defect234556002
- Specific antibody deficiency234556002
- Specific immunoglobulin response defect234556002
- Congenital hypogammaglobulinaemia267460002
- Congenital hypogammaglobulinemia267460002
- X-linked intellectual disability with hypogammaglobulinaemia and progressive neurological deterioration syndrome719156006
- X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome719156006
- Microcephaly, hypogammaglobulinaemia, abnormal immunity syndrome721903007
- Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome721903007
- Say Barber Miller syndrome721903007
- Agammaglobulinaemia, microcephaly, craniosynostosis, severe dermatitis syndrome722281001
- Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome722281001
- Isolated agammaglobulinaemia764858009
- Isolated agammaglobulinemia764858009
- Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinaemia773730002
- Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia773730002
- Autosomal recessive osteopetrosis type 7773730002
- Osteopetrosis hypogammaglobulinaemia syndrome773730002
- Osteopetrosis hypogammaglobulinemia syndrome773730002
- 2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia1197476009
- 2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia1197476009
- Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia1197476009
- Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia1197476009
- OAS1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia1197476009
- OAS1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia1197476009
- Agammaglobulinaemia due to TOP2B mutation1230295000
- Agammaglobulinemia due to TOP2B mutation1230295000
- B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome1230295000
- BILU (B-cell immunodeficiency, limb, urogenital) syndrome1230295000
- BILU syndrome1230295000
- Hoffman syndrome due to TOP2B deficiency1230295000
- Autosomal recessive agammaglobulinaemia1297036006
- Autosomal recessive agammaglobulinemia1297036006
- Agammaglobulinaemia due to SPI1 defect1351647002
- Agammaglobulinemia due to SPI1 defect1351647002
- Autosomal dominant agammaglobulinaemia due to PU.1 deficiency1351647002
- Autosomal dominant agammaglobulinemia due to PU.1 deficiency1351647002
- Agammaglobulinaemia due to FNIP1 defect1351648007
- Agammaglobulinemia due to FNIP1 defect1351648007
- Autosomal recessive agammaglobulinaemia due to FNIP1 deficiency1351648007
- Autosomal recessive agammaglobulinaemia due to folliculin interacting protein 1 deficiency1351648007
- Autosomal recessive agammaglobulinemia due to FNIP1 deficiency1351648007
- Autosomal recessive agammaglobulinemia due to folliculin interacting protein 1 deficiency1351648007
- Autosomal recessive agammaglobulinaemia due to SLC39A7 deficiency1351665003
- Autosomal recessive agammaglobulinaemia due to solute carrier family 39 member 7 deficiency1351665003
- Autosomal recessive agammaglobulinemia due to SLC39A7 deficiency1351665003
- Autosomal recessive agammaglobulinemia due to solute carrier family 39 member 7 deficiency1351665003
- Autosomal recessive agammaglobulinaemia due to E47 transcription factor deficiency1351667006
- Autosomal recessive agammaglobulinaemia due to TCF3 mutation1351667006
- Autosomal recessive agammaglobulinemia due to E47 transcription factor deficiency1351667006
- Autosomal recessive agammaglobulinemia due to TCF3 mutation1351667006
- Autosomal dominant agammaglobulinaemia due to E47 transcription factor deficiency1351668001
- Autosomal dominant agammaglobulinaemia due to TCF3 mutation1351668001
- Autosomal dominant agammaglobulinemia due to E47 transcription factor deficiency1351668001
- Autosomal dominant agammaglobulinemia due to TCF3 mutation1351668001
- Autosomal recessive agammaglobulinaemia due to PIK3R1 mutation1351669009
- Autosomal recessive agammaglobulinaemia due to p85 deficiency1351669009
- Autosomal recessive agammaglobulinemia due to PIK3R1 mutation1351669009
- Autosomal recessive agammaglobulinemia due to p85 deficiency1351669009
- Autosomal recessive agammaglobulinaemia due to PIK3CD mutation1351670005
- Autosomal recessive agammaglobulinaemia due to p110 delta deficiency1351670005
- Autosomal recessive agammaglobulinemia due to PIK3CD mutation1351670005
- Autosomal recessive agammaglobulinemia due to p110 delta deficiency1351670005
- Autosomal recessive agammaglobulinaemia due to B cell linker deficiency1351671009
- Autosomal recessive agammaglobulinaemia due to BLNK deficiency1351671009
- Autosomal recessive agammaglobulinaemia due to BLNK mutation1351671009
- Autosomal recessive agammaglobulinemia due to B cell linker deficiency1351671009
- Autosomal recessive agammaglobulinemia due to BLNK deficiency1351671009
- Autosomal recessive agammaglobulinemia due to BLNK mutation1351671009
- Autosomal recessive agammaglobulinaemia due to IGLL1 mutation1351672002
- Autosomal recessive agammaglobulinaemia due to lambda 5 deficiency1351672002
- Autosomal recessive agammaglobulinemia due to IGLL1 mutation1351672002
- Autosomal recessive agammaglobulinemia due to lambda 5 deficiency1351672002
- Autosomal recessive agammaglobulinaemia due to IGHM mutation1351675000
- Autosomal recessive agammaglobulinaemia due to immunoglobulin heavy chain mu constant region deficiency1351675000
- Autosomal recessive agammaglobulinemia due to IGHM mutation1351675000
- Autosomal recessive agammaglobulinemia due to immunoglobulin heavy chain mu constant region deficiency1351675000
- Autosomal recessive agammaglobulinaemia due to CD79B mutation1351678003
- Autosomal recessive agammaglobulinaemia due to immunoglobulin beta deficiency1351678003
- Autosomal recessive agammaglobulinemia due to CD79B mutation1351678003
- Autosomal recessive agammaglobulinemia due to immunoglobulin beta deficiency1351678003
- Autosomal recessive agammaglobulinaemia due to CD79A mutation1351679006
- Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha deficiency1351679006
- Autosomal recessive agammaglobulinemia due to CD79A mutation1351679006
- Autosomal recessive agammaglobulinemia due to immunoglobulin alpha deficiency1351679006
Frequently Asked Questions
What is ICD-10 code D80.0?
ICD-10-CM code D80.0 represents "Hereditary hypogammaglobulinemia". It is a billable/specific code that can be used on a claim.
Is D80.0 a billable code?
Yes, D80.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D80.0 in?
D80.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D80.0?
D80.0 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).
What SNOMED CT codes does D80.0 map to?
D80.0 maps to 29 SNOMED CT concepts: 1197476009, 1351648007, 1351647002, 1230295000, 722281001, and 24 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D80.0?
D80.0 is linked to 3 UMLS Concept Unique Identifiers: C2873841, C0494249, C2873842. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.