E70.330
BillableChediak-Higashi syndrome
Chediak-Higashi syndrome
Coding Notes
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
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
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
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.
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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.