E70.330
BillableChediak-Higashi syndrome
Chediak-Higashi syndrome
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(3)
Also Known As / Clinical Terms(85)
SNOMED CT
- Partial albinism6479008
- Beguez Cesar disease111396008
- Béguez César disease111396008
- Chediak Higashi syndrome111396008
- Chediak anomaly111396008
- Chediak-Higashi syndrome111396008
- Chediak-Steinbrinck anomaly111396008
- Chediak-Steinbrinck-Higashi syndrome111396008
- Chédiak anomaly111396008
- Chédiak-Higashi syndrome111396008
- Chédiak-Steinbrinck anomaly111396008
- Congenital gigantism of peroxidase granules111396008
- Granulation anomaly of leucocytes111396008
- Granulation anomaly of leukocytes111396008
- Hereditary gigantism of cytoplasmic organelles111396008
- Hereditary leukomelanopathy111396008
- Steinbrinck anomaly111396008
- Chemotactic disorder234429002
- Dense body defect234474009
- Storage pool deficiency234474009
- Granulocyte granule deficiency289317009
- Attenuated Chédiak-Higashi syndrome720520009
- Atypical Chédiak-Higashi syndrome720520009
- Periodontitis exacerbated by Chédiak-Higashi syndrome1187148008
UMLS
- Begnez Cesar diseaseC0007965
- Beguez Cesar diseaseC0007965
- Béguez César diseaseC0007965
- CHEDIAK-HIGASHI SYNDROMEC0007965
- CHSC0007965
- Chediak Higashi SyndromeC0007965
- Chediak Higashi anomalyC0007965
- Chediak Higashi syndromeC0007965
- Chediak Steinbrinck Higashi SyndromeC0007965
- Chediak anomalyC0007965
- Chediak-Higashi SyndromeC0007965
- Chediak-Higashi syndromeC0007965
- Chediak-Steinbrinck anomalyC0007965
- Chediak-Steinbrinck-Higashi SyndromeC0007965
- Chediak-Steinbrinck-Higashi SyndromesC0007965
- Chediak-Steinbrinck-Higashi syndromeC0007965
- Chédiak anomalyC0007965
- Chédiak-Higashi syndromeC0007965
- Chédiak-Higashi syndrome (disorder)C0007965
- Chédiak-Steinbrinck anomalyC0007965
- Congenital gigantism of peroxidase granulesC0007965
- Granulation anomaly of leucocytesC0007965
- Granulation anomaly of leukocytesC0007965
- Hereditary gigantism of cytoplasmic organellesC0007965
- Hereditary leukomelanopathyC0007965
- Oculocutaneous Albinism with Leukocyte DefectC0007965
- Oculocutaneous albinism with leukocyte defectC0007965
- Steinbrinck anomalyC0007965
- chediak higashi anomalyC0007965
- chediak higashi syndromeC0007965
- chediak-higashi syndromeC0007965
Clinical Terms
- Atypical Chédiak-Higashi syndrome
- Hereditary leukomelanopathy
- Periodontitis exacerbated by Chédiak-Higashi syndrome
- Chediak-Steinbrinck-Higashi Syndromes
- Begnez Cesar disease
- Oculocutaneous Albinism with Leukocyte Defect
- Congenital gigantism of peroxidase granules
- Chédiak-Steinbrinck anomaly
- Chediak Higashi anomaly
- CHS
- Chediak Higashi syndrome
- Chediak-Steinbrinck-Higashi Syndrome
- Chediak Steinbrinck Higashi Syndrome
- Béguez César disease
- Hereditary gigantism of cytoplasmic organelles
- Storage pool deficiency
- Steinbrinck anomaly
- Partial albinism
- Granulation anomaly of leucocytes
- Chediak anomaly
- Chédiak-Higashi syndrome
- Chédiak-Higashi syndrome (disorder)
- Attenuated Chédiak-Higashi syndrome
- Dense body defect
- Granulation anomaly of leukocytes
- Chemotactic disorder
- Granulocyte granule deficiency
- Chediak-Steinbrinck anomaly
- Beguez Cesar disease
- Chédiak anomaly
Frequently Asked Questions
What is the ICD-10 code for chediak-higashi syndrome?
The ICD-10-CM code for chediak-higashi syndrome is E70.330. The full clinical description is "Chediak-Higashi syndrome". E70.330 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E70.330 mean?
ICD-10-CM code E70.330 represents “Chediak-Higashi syndrome”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E70.330 a billable code?
Yes, E70.330 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E70.330 in?
E70.330 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E70.330?
E70.330 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 3 more.
What SNOMED CT codes does E70.330 map to?
E70.330 maps to 7 SNOMED CT concepts: 720520009, 111396008, 234429002, 234474009, 289317009, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E70.330?
E70.330 is linked to 1 UMLS Concept Unique Identifier: C0007965. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E70.330 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like chediak-higashi 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 E70.330?
There is no direct ICD-11 mapping available for E70.330 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.