E70.39
BillableOther specified albinism
Other specified albinism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Piebaldism
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
- Chediak-Higashi-like syndrome37548006
- Griscelli syndrome37548006
- Griscelli syndrome with immunodeficiency37548006
- Hypopigmentation-immunodeficiency disease37548006
- Partial albinism with immunodeficiency37548006
- Waardenburg syndrome47434006
- Waardenburg's syndrome47434006
- Sensorineural hearing loss of bilateral ears194424005
- Sensorineural hearing loss of both ears194424005
- Immunodeficiency with major anomalies234631003
- Immunodeficiency associated with multiple organ system abnormalities234641000
- Klein-Waardenberg syndrome237918004
- Klein-Waardenberg's syndrome237918004
- Waardenburg syndrome type 3237918004
- Waardenburg syndrome type III237918004
- Waardenburg syndrome with limb anomalies237918004
- Albinism-deafness syndrome of Tietz403805009
- Ziprkowski-Margolis syndrome403806005
- Phylloid hypomelanosis403807001
- Dead ear700454004
- Profound sensorineural hearing loss700454004
- Piebaldism718122005
- Dystopia canthorum726407000
- Piebald trait with neurologic defects syndrome773984007
- Telfer Sugar Jaeger syndrome773984007
- Profound hearing loss1230412003
- Griscelli syndrome type 11254946006
- Hypopigmentation-immunodeficiency disease type 11254946006
- Griscelli syndrome type 31254947002
- Hypopigmentation-immunodeficiency disease type 31254947002
UMLS
- Other specified albinismC2874233
- PBTC0080024
- PIEBALD TRAITC0080024
- PIEBALDISMC0080024
- Piebald TraitC0080024
- Piebald TraitsC0080024
- Piebald skin depigmentationC0080024
- Piebald traitC0080024
- PiebaldismC0080024
- Piebaldism (disorder)C0080024
- Trait, PiebaldC0080024
- Traits, PiebaldC0080024
- partial albinismC0080024
- piebaldismC0080024
Frequently Asked Questions
What is the ICD-10 code for other specified albinism?
The ICD-10-CM code for other specified albinism is E70.39. The full clinical description is "Other specified albinism". E70.39 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E70.39 mean?
ICD-10-CM code E70.39 represents "Other specified albinism". 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 E70.39 a billable code?
Yes, E70.39 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E70.39 in?
E70.39 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E70.39?
E70.39 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 E70.39 map to?
E70.39 maps to 16 SNOMED CT concepts: 403805009, 37548006, 700454004, 726407000, 1254946006, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E70.39?
E70.39 is linked to 2 UMLS Concept Unique Identifiers: C2874233, C0080024. 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.